Correction to: Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case report

Jaber Lyahyai
Bouchra Ouled Amar Bencheikh
Siham C. Elalaoui
Maria Mansouri
Lamia Boualla
Alexandre DIonne-Laporte
Dan Spiegelman
Patrick A. Dion
Patrick Cossette
Guy A. Rouleau
Abdelaziz Sefiani

Open link

Publication date

April 2018

DOI

10.1186/s12887-018-1114-y

Publisher

Springer Science and Business Media LLC

Journal

BMC Pediatrics

Abstract

After publication of the original article [1] it was brought to our attention that author Bouchra Ouled Amar Bencheikh was incorrectly included as Bouchra Oulad Amar Bencheikh

Extracted data

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Data Protection

Correction to: Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case report

Jaber Lyahyai
Bouchra Ouled Amar Bencheikh
Siham C. Elalaoui
Maria Mansouri
Lamia Boualla
Alexandre DIonne-Laporte
Dan Spiegelman
Patrick A. Dion
Patrick Cossette
Guy A. Rouleau
Abdelaziz Sefiani

Open link

Publication date

April 2018

DOI

10.1186/s12887-018-1114-y

Publisher

Springer Science and Business Media LLC

Journal

BMC Pediatrics

Abstract

After publication of the original article [1] it was brought to our attention that author Bouchra Ouled Amar Bencheikh was incorrectly included as Bouchra Oulad Amar Bencheikh

Extracted data

Riazuddin, S.
Hussain, M.
Razzaq, A.
Iqbal, Z.
Shahzad, M.
Polla, D.L.
Song, Y.
van Beusekom, E.
Khan, A.A.
Tomas-Roca, L.
Rashid, M.
Zahoor, M.Y.
Wissink-Lindhout, W.M.
Basra, M.A.R.
Ansar, M.
Agha, Z.
van Heeswijk, K.
Rasheed, F.
Van de Vorst, M.
Veltman, J.A.
Gilissen, C.
Akram, J.
Kleefstra, T.
Assir, M.Z.
Grozeva, D.
Carss, K.
Raymond, F.L.
O'Connor, T.D.
Riazuddin, S.A.
Khan, S.N.
Ahmed, Z.M.
de Brouwer, A.P.M.
van Bokhoven, H.
UK10K, U.K.1.0.K.

November 2020

This Article was originally published under a CC BY-NC-SA 4.0 license, but has now been made availab...

Correction: Clinical and genetic characterization of chanarin-dorfman syndrome patients: first report of large deletions in the ABHD5 gene

Redaelli, Chiara
Coleman, Rosalind
Moro, Laura
Sertedaki, Amalia
Kakourou, Talia
Elsayed, Solaf
Prati, Daniele
Colli, Agostino
Mela, Donatella
Colombo, Roberto
Tavian, Daniela

February 2011

AbstractFollowing the publication of this article [Redaelli C et al, Clinical and genetic characteri...

Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis (European Journal of Human Genetics, (2021), 29, 9, (1359-1368), 10.1038/s41431-021-00900-2)

de Boer E.
Ockeloen C. W.
Matalonga L.
Horvath R.
Cohen E.
Cuesta I.
Danis D.
Denomme-Pichon A. -S.
Duffourd Y.
Gilissen C.
Johari M.
Laurie S.
Li S.
Matalonga L.
Nelson I.
Peters S.
Paramonov I.
Prasanth S.
Robinson P.
Sablauskas K.
Savarese M.
Steyaert W.
Topf A.
van der Velde J. K.
Vitobello A.
Rodenburg R. J.
Coenen M. J. H.
Janssen M.
Henssen D.
Gilissen C.
Steyaert W.
Paramonov I.
Banka S.
Benetti E.
Casari G.
Ciolfi A.
Clayton-Smith J.
Dallapiccola B.
de Boer E.
Faivre L.
Haack T. B.
Hammarsjo A.
Havlovicova M.
Hoischen A.
Hugon A.
Jackson A.
Kleefstra T.
Lindstrand A.
Lopez-Martin E.
Macek M.
Nigro V.
Nordgren A.
Pettersson M.
Pinelli M.
Pizzi S.
Posada M.
Radio F. C.
Renieri A.
Rooryck C.
Ryba L.
Schwarz M.
Tartaglia M.
Thauvin C.
Torella A.
Verloes A.
Vissers L.
Vyshka K.
Zurek B.
Trimouille A.
Kleefstra T.
Verloes A.
Vissers L. E. L. M.

January 2021

In the original publication of the article, consortium author lists were missing in the article. The...

Correction to: Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population

Arshi Naz
Arijit Biswas
Tehmina Nafees Khan
Anne Goodeve
Nisar Ahmed
Nazish Saqlain
Shariq Ahmed
Ikram Din Ujjan
Tahir S. Shamsi
Johannes Oldenburg

April 2019

Following the publication of this article [1], the authors noted the following typographical errors

Correction to: High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry (neurogenetics, (2023), 10.1007/s10048-023-00730-y)

Ashrafi, M.
Kameli, R.
Hosseinpour, S.
Razmara, E.
Zamani, Z.
Rezaei, Z.
Mashayekhi, R.
Pak, N.
Barzegar, M.
Azizimalamiri, R.
Kashani, M. R.
Khosroshahi, N.
Rasulinezhad, M.
Heidari, M.
Amanat, M.
Abdi, A.
Mohammadi, B.
Mohammadi, M.
Zamani, G. R.
Badv, R. S.
Omrani, A.
Nikbakht, S.
Bereshneh, A. H.
Movahedinia, M.
Moghaddam, H. F.
Ardakani, H. S.
Akbari, M. G.
Tousi, M. B.
Shahi, M. V.
Hosseini, F.
Amouzadeh, M. H.
Hosseini, S. A.
Nikkhah, A.
Khajeh, A.
Alizadeh, H.
Yarali, B.
Rohani, M.
Karimi, P.
Elahi, H. M. L.
Hosseiny, S. M. M.
Sadeghzadeh, M. S.
Mohebbi, H.
Moghadam, M. H.
Aryan, H.
Vahidnezhad, H.
Soveizi, M.
Rabbani, B.
Rabbani, A.
Mahdieh, N.
Garshasbi, M.
Tavasoli, A. R.

January 2023

The published online version of the original article contains a mistake. The authors would like to c...

Author Correction: Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome

Vabres, Pierre
Sorlin, Arthur
Kholmanskikh, Stanislav S.
Demeer, Bénédicte
St Onge, Judith
Duffourd, Yannis
Kuentz, Paul
Courcet, Jean-Benoît
Carmignac, Virginie
Garret, Philippine
Bessis, Didier
Boute, Odile
Bron, Alain
Captier, Guillaume
Carmi, Esther
Devauchelle, Bernard
Geneviève, David
Gondry Jouet, Catherine
Guibaud, Laurent
Lafon, Arnaud
Mathieu Dramard, Michèle
Thevenon, Julien
Dobyns, William B.
Bernard, Geneviève
Polubothu, Satyamaanasa
Faravelli, Francesca
Kinsler, Veronica A.
Thauvin, Christel
Faivre, Laurence
Ross, Elizabeth M.
Rivière, Jean-Baptiste

January 2019

Published Erratum: Correction to: Nature Genetics 51: 1438–1441 https://doi.org/10.1038/s41588-019-0...

Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome (Genetics in Medicine, (2019), 21, 6, (1295-1307), 10.1038/s41436-018-0330-z)

van der Sluijs, Pleuntje J.
Jansen, Sandra
Vergano, Samantha A.
Adachi-Fukuda, Miho
Alanay, Yasemin
AlKindy, Adila
Baban, Anwar
Bayat, Allan
Beck-Wödl, Stefanie
Berry, Katherine
Bijlsma, Emilia K.
Bok, Levinus A.
Brouwer, Alwin F. J.
van der Burgt, Ineke
Campeau, Philippe M.
Canham, Natalie
Chrzanowska, Krystyna
Chu, Yoyo W. Y.
Chung, Brain H. Y.
Dahan, Karin
de Rademaeker, Marjan
Destree, Anne
Dudding-Byth, Tracy
Earl, Rachel
Elcioglu, Nursel
Elias, Ellen R.
Fagerberg, Christina
Gardham, Alice
Gener, Blanca
Gerkes, Erica H.
Grasshoff, Ute
van Haeringen, Arie
Heitink, Karin R.
Herkert, Johanna C.
den Hollander, Nicolette S.
Horn, Denise
Hunt, David
Kant, Sarina G.
Kato, Mitsuhiro
Kayserili, H. lya
Kersseboom, Rogier
Kilic, Esra
Krajewska-Walasek, Malgorzata
Lammers, Kylin
Laulund, Lone W.
Lederer, Damien
Lees, Melissa
López-González, Vanesa
Maas, Saskia
Mancini, Grazia M. S.
Marcelis, Carlo
Martinez, Francisco
Maystadt, Isabelle
McGuire, Marianne
McKee, Shane
Mehta, Sarju
Metcalfe, Kay
Milunsky, Jeff
Mizuno, Seiji
Moeschler, John B.
Netzer, Christian
Ockeloen, Charlotte W.
Oehl-Jaschkowitz, Barbara
Okamoto, Nobuhiko
Olminkhof, Sharon N. M.
Orellana, Carmen
Pasquier, Laurent
Pottinger, Caroline
Riehmer, Vera
Robertson, Stephen P.
Roifman, Maian
Rooryck, Caroline
Ropers, Fabienne G.
Rosello, Monica
Ruivenkamp, Claudia A. L.
Sagiroglu, Mahmut S.
Sallevelt, Suzanne C. E. H.
Calvo, Amparo Sanchis
Simsek-Kiper, Pelin O.
Soares, Gabriela
Solaeche, Lucia
Sonmez, Fatma Mujgan
Splitt, Miranda
Steenbeek, Duco
Stegmann, Alexander P. A.
Stumpel, Constance T. R. M.
Tanabe, Saori
Uctepe, Eyyup
Utine, G. Eda
Veenstra-Knol, Hermine E.
Venkateswaran, Sunita
Vilain, Catheline
Vincent-Delorme, Catherine
Vulto-van Silfhout, Anneke T.
Wheeler, Patricia
Wilson, Golder N.
Wilson, Louise C.
Wollnik, Bernd
Kosho, Tomoki
Wieczorek, Dagmar
Eichler, Evan
Pfundt, Rolph
de Vries, Bert B. A.
Clayton-Smith, Jill
Santen, Gijs W. E.

September 2019

The original version of this Article contained an error in the spelling of the author Pleuntje J. va...

Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome (Genetics in Medicine, (2018), 10.1038/s41436-018-0330-z)

van der Sluijs, Pleuntje J.
Jansen, Sandra
Vergano, Samantha A.
Adachi-Fukuda, Miho
Alanay, Yasemin
AlKindy, Adila
Baban, Anwar
Bayat, Allan
Beck-Wödl, Stefanie
Berry, Katherine
Bijlsma, Emilia K.
Bok, Levinus A.
Brouwer, Alwin F. J.
van der Burgt, Ineke
Campeau, Philippe M.
Canham, Natalie
Chrzanowska, Krystyna
Chu, Yoyo W. Y.
Chung, Brain H. Y.
Dahan, Karin
de Rademaeker, Marjan
Destree, Anne
Dudding-Byth, Tracy
Earl, Rachel
Elcioglu, Nursel
Elias, Ellen R.
Fagerberg, Christina
Gardham, Alice
Gener, Blanca
Gerkes, Erica H.
Grasshoff, Ute
van Haeringen, Arie
Heitink, Karin R.
Herkert, Johanna C.
den Hollander, Nicolette S.
Horn, Denise
Hunt, David
Kant, Sarina G.
Kato, Mitsuhiro
Kayserili, H. lya
Kersseboom, Rogier
Kilic, Esra
Krajewska-Walasek, Malgorzata
Lammers, Kylin
Laulund, Lone W.
Lederer, Damien
Lees, Melissa
López-González, Vanesa
Maas, Saskia
Mancini, Grazia M. S.
Marcelis, Carlo
Martinez, Francisco
Maystadt, Isabelle
McGuire, Marianne
McKee, Shane
Mehta, Sarju
Metcalfe, Kay
Milunsky, Jeff
Mizuno, Seiji
Moeschler, John B.
Netzer, Christian
Ockeloen, Charlotte W.
Oehl-Jaschkowitz, Barbara
Okamoto, Nobuhiko
Olminkhof, Sharon N. M.
Orellana, Carmen
Pasquier, Laurent
Pottinger, Caroline
Riehmer, Vera
Robertson, Stephen P.
Roifman, Maian
Rooryck, Caroline
Ropers, Fabienne G.
Rosello, Monica
Ruivenkamp, Claudia A. L.
Sagiroglu, Mahmut S.
Sallevelt, Suzanne C. E. H.
Calvo, Amparo Sanchis
Simsek-Kiper, Pelin O.
Soares, Gabriela
Solaeche, Lucia
Sonmez, Fatma Mujgan
Splitt, Miranda
Steenbeek, Duco
Stegmann, Alexander P. A.
Stumpel, Constance T. R. M.
Tanabe, Saori
Uctepe, Eyyup
Utine, G. Eda
Veenstra-Knol, Hermine E.
Venkateswaran, Sunita
Vilain, Catheline
Vincent-Delorme, Catherine
Vulto-van Silfhout, Anneke T.
Wheeler, Patricia
Wilson, Golder N.
Wilson, Louise C.
Wollnik, Bernd
Kosho, Tomoki
Wieczorek, Dagmar
Eichler, Evan
Pfundt, Rolph
de Vries, Bert B. A.
Clayton-Smith, Jill
Santen, Gijs W. E.

September 2019

The original version of this Article contained an error in the spelling of the author Pleuntje J. va...

Publisher correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways

Duffy, David L.
Zhu, Gu
Li, Xin
Sanna, Marianna
Iles, Mark M.
Jacobs, Leonie C.
Evans, David M.
Yazar, Seyhan
Beesley, Jonathan
Law, Matthew H.
Kraft, Peter
Visconti, Alessia
Taylor, John C.
Liu, Fan
Wright, Margaret J.
Henders, Anjali K.
Bowdler, Lisa
Glass, Dan
Ikram, M. Arfan
Uitterlinden, André G.
Madden, Pamela A.
Heath, Andrew C.
Nelson, Elliot C.
Green, Adele C.
Chanock, Stephen
Barrett, Jennifer H.
Brown, Matthew A.
Hayward, Nicholas K.
MacGregor, Stuart
Sturm, Richard A.
Hewitt, Alex W.

January 2019

The original version of this Article contained errors in the spelling of the authors Fan Liu and M. ...

Correction: Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability

Riazuddin, S.
Hussain, M.
Razzaq, A.
Iqbal, Z.
Shahzad, M.
Polla, D.L.
Song, Y.
van Beusekom, E.
Khan, A.A.
Tomas-Roca, L.
Rashid, M.
Zahoor, M.Y.
Wissink-Lindhout, W.M.
Basra, M.A.R.
Ansar, M.
Agha, Z.
van Heeswijk, K.
Rasheed, F.
Van de Vorst, M.
Veltman, J.A.
Gilissen, C.
Akram, J.
Kleefstra, T.
Assir, M.Z.
Grozeva, D.
Carss, K.
Raymond, F.L.
O'Connor, T.D.
Riazuddin, S.A.
Khan, S.N.
Ahmed, Z.M.
de Brouwer, A.P.M.
van Bokhoven, H.
UK10K, U.K.1.0.K.

November 2020

This Article was originally published under a CC BY-NC-SA 4.0 license, but has now been made availab...

Correction: Clinical and genetic characterization of chanarin-dorfman syndrome patients: first report of large deletions in the ABHD5 gene

Redaelli, Chiara
Coleman, Rosalind
Moro, Laura
Sertedaki, Amalia
Kakourou, Talia
Elsayed, Solaf
Prati, Daniele
Colli, Agostino
Mela, Donatella
Colombo, Roberto
Tavian, Daniela

February 2011

AbstractFollowing the publication of this article [Redaelli C et al, Clinical and genetic characteri...

de Boer E.
Ockeloen C. W.
Matalonga L.
Horvath R.
Cohen E.
Cuesta I.
Danis D.
Denomme-Pichon A. -S.
Duffourd Y.
Gilissen C.
Johari M.
Laurie S.
Li S.
Matalonga L.
Nelson I.
Peters S.
Paramonov I.
Prasanth S.
Robinson P.
Sablauskas K.
Savarese M.
Steyaert W.
Topf A.
van der Velde J. K.
Vitobello A.
Rodenburg R. J.
Coenen M. J. H.
Janssen M.
Henssen D.
Gilissen C.
Steyaert W.
Paramonov I.
Banka S.
Benetti E.
Casari G.
Ciolfi A.
Clayton-Smith J.
Dallapiccola B.
de Boer E.
Faivre L.
Haack T. B.
Hammarsjo A.
Havlovicova M.
Hoischen A.
Hugon A.
Jackson A.
Kleefstra T.
Lindstrand A.
Lopez-Martin E.
Macek M.
Nigro V.
Nordgren A.
Pettersson M.
Pinelli M.
Pizzi S.
Posada M.
Radio F. C.
Renieri A.
Rooryck C.
Ryba L.
Schwarz M.
Tartaglia M.
Thauvin C.
Torella A.
Verloes A.
Vissers L.
Vyshka K.
Zurek B.
Trimouille A.
Kleefstra T.
Verloes A.
Vissers L. E. L. M.

January 2021

In the original publication of the article, consortium author lists were missing in the article. The...

Correction to: Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population

Arshi Naz
Arijit Biswas
Tehmina Nafees Khan
Anne Goodeve
Nisar Ahmed
Nazish Saqlain
Shariq Ahmed
Ikram Din Ujjan
Tahir S. Shamsi
Johannes Oldenburg

April 2019

Following the publication of this article [1], the authors noted the following typographical errors

Correction to: High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry (neurogenetics, (2023), 10.1007/s10048-023-00730-y)

Ashrafi, M.
Kameli, R.
Hosseinpour, S.
Razmara, E.
Zamani, Z.
Rezaei, Z.
Mashayekhi, R.
Pak, N.
Barzegar, M.
Azizimalamiri, R.
Kashani, M. R.
Khosroshahi, N.
Rasulinezhad, M.
Heidari, M.
Amanat, M.
Abdi, A.
Mohammadi, B.
Mohammadi, M.
Zamani, G. R.
Badv, R. S.
Omrani, A.
Nikbakht, S.
Bereshneh, A. H.
Movahedinia, M.
Moghaddam, H. F.
Ardakani, H. S.
Akbari, M. G.
Tousi, M. B.
Shahi, M. V.
Hosseini, F.
Amouzadeh, M. H.
Hosseini, S. A.
Nikkhah, A.
Khajeh, A.
Alizadeh, H.
Yarali, B.
Rohani, M.
Karimi, P.
Elahi, H. M. L.
Hosseiny, S. M. M.
Sadeghzadeh, M. S.
Mohebbi, H.
Moghadam, M. H.
Aryan, H.
Vahidnezhad, H.
Soveizi, M.
Rabbani, B.
Rabbani, A.
Mahdieh, N.
Garshasbi, M.
Tavasoli, A. R.

January 2023

The published online version of the original article contains a mistake. The authors would like to c...

Author Correction: Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome

Vabres, Pierre
Sorlin, Arthur
Kholmanskikh, Stanislav S.
Demeer, Bénédicte
St Onge, Judith
Duffourd, Yannis
Kuentz, Paul
Courcet, Jean-Benoît
Carmignac, Virginie
Garret, Philippine
Bessis, Didier
Boute, Odile
Bron, Alain
Captier, Guillaume
Carmi, Esther
Devauchelle, Bernard
Geneviève, David
Gondry Jouet, Catherine
Guibaud, Laurent
Lafon, Arnaud
Mathieu Dramard, Michèle
Thevenon, Julien
Dobyns, William B.
Bernard, Geneviève
Polubothu, Satyamaanasa
Faravelli, Francesca
Kinsler, Veronica A.
Thauvin, Christel
Faivre, Laurence
Ross, Elizabeth M.
Rivière, Jean-Baptiste

January 2019

Published Erratum: Correction to: Nature Genetics 51: 1438–1441 https://doi.org/10.1038/s41588-019-0...

Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome (Genetics in Medicine, (2019), 21, 6, (1295-1307), 10.1038/s41436-018-0330-z)

van der Sluijs, Pleuntje J.
Jansen, Sandra
Vergano, Samantha A.
Adachi-Fukuda, Miho
Alanay, Yasemin
AlKindy, Adila
Baban, Anwar
Bayat, Allan
Beck-Wödl, Stefanie
Berry, Katherine
Bijlsma, Emilia K.
Bok, Levinus A.
Brouwer, Alwin F. J.
van der Burgt, Ineke
Campeau, Philippe M.
Canham, Natalie
Chrzanowska, Krystyna
Chu, Yoyo W. Y.
Chung, Brain H. Y.
Dahan, Karin
de Rademaeker, Marjan
Destree, Anne
Dudding-Byth, Tracy
Earl, Rachel
Elcioglu, Nursel
Elias, Ellen R.
Fagerberg, Christina
Gardham, Alice
Gener, Blanca
Gerkes, Erica H.
Grasshoff, Ute
van Haeringen, Arie
Heitink, Karin R.
Herkert, Johanna C.
den Hollander, Nicolette S.
Horn, Denise
Hunt, David
Kant, Sarina G.
Kato, Mitsuhiro
Kayserili, H. lya
Kersseboom, Rogier
Kilic, Esra
Krajewska-Walasek, Malgorzata
Lammers, Kylin
Laulund, Lone W.
Lederer, Damien
Lees, Melissa
López-González, Vanesa
Maas, Saskia
Mancini, Grazia M. S.
Marcelis, Carlo
Martinez, Francisco
Maystadt, Isabelle
McGuire, Marianne
McKee, Shane
Mehta, Sarju
Metcalfe, Kay
Milunsky, Jeff
Mizuno, Seiji
Moeschler, John B.
Netzer, Christian
Ockeloen, Charlotte W.
Oehl-Jaschkowitz, Barbara
Okamoto, Nobuhiko
Olminkhof, Sharon N. M.
Orellana, Carmen
Pasquier, Laurent
Pottinger, Caroline
Riehmer, Vera
Robertson, Stephen P.
Roifman, Maian
Rooryck, Caroline
Ropers, Fabienne G.
Rosello, Monica
Ruivenkamp, Claudia A. L.
Sagiroglu, Mahmut S.
Sallevelt, Suzanne C. E. H.
Calvo, Amparo Sanchis
Simsek-Kiper, Pelin O.
Soares, Gabriela
Solaeche, Lucia
Sonmez, Fatma Mujgan
Splitt, Miranda
Steenbeek, Duco
Stegmann, Alexander P. A.
Stumpel, Constance T. R. M.
Tanabe, Saori
Uctepe, Eyyup
Utine, G. Eda
Veenstra-Knol, Hermine E.
Venkateswaran, Sunita
Vilain, Catheline
Vincent-Delorme, Catherine
Vulto-van Silfhout, Anneke T.
Wheeler, Patricia
Wilson, Golder N.
Wilson, Louise C.
Wollnik, Bernd
Kosho, Tomoki
Wieczorek, Dagmar
Eichler, Evan
Pfundt, Rolph
de Vries, Bert B. A.
Clayton-Smith, Jill
Santen, Gijs W. E.

September 2019

The original version of this Article contained an error in the spelling of the author Pleuntje J. va...

Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome (Genetics in Medicine, (2018), 10.1038/s41436-018-0330-z)

van der Sluijs, Pleuntje J.
Jansen, Sandra
Vergano, Samantha A.
Adachi-Fukuda, Miho
Alanay, Yasemin
AlKindy, Adila
Baban, Anwar
Bayat, Allan
Beck-Wödl, Stefanie
Berry, Katherine
Bijlsma, Emilia K.
Bok, Levinus A.
Brouwer, Alwin F. J.
van der Burgt, Ineke
Campeau, Philippe M.
Canham, Natalie
Chrzanowska, Krystyna
Chu, Yoyo W. Y.
Chung, Brain H. Y.
Dahan, Karin
de Rademaeker, Marjan
Destree, Anne
Dudding-Byth, Tracy
Earl, Rachel
Elcioglu, Nursel
Elias, Ellen R.
Fagerberg, Christina
Gardham, Alice
Gener, Blanca
Gerkes, Erica H.
Grasshoff, Ute
van Haeringen, Arie
Heitink, Karin R.
Herkert, Johanna C.
den Hollander, Nicolette S.
Horn, Denise
Hunt, David
Kant, Sarina G.
Kato, Mitsuhiro
Kayserili, H. lya
Kersseboom, Rogier
Kilic, Esra
Krajewska-Walasek, Malgorzata
Lammers, Kylin
Laulund, Lone W.
Lederer, Damien
Lees, Melissa
López-González, Vanesa
Maas, Saskia
Mancini, Grazia M. S.
Marcelis, Carlo
Martinez, Francisco
Maystadt, Isabelle
McGuire, Marianne
McKee, Shane
Mehta, Sarju
Metcalfe, Kay
Milunsky, Jeff
Mizuno, Seiji
Moeschler, John B.
Netzer, Christian
Ockeloen, Charlotte W.
Oehl-Jaschkowitz, Barbara
Okamoto, Nobuhiko
Olminkhof, Sharon N. M.
Orellana, Carmen
Pasquier, Laurent
Pottinger, Caroline
Riehmer, Vera
Robertson, Stephen P.
Roifman, Maian
Rooryck, Caroline
Ropers, Fabienne G.
Rosello, Monica
Ruivenkamp, Claudia A. L.
Sagiroglu, Mahmut S.
Sallevelt, Suzanne C. E. H.
Calvo, Amparo Sanchis
Simsek-Kiper, Pelin O.
Soares, Gabriela
Solaeche, Lucia
Sonmez, Fatma Mujgan
Splitt, Miranda
Steenbeek, Duco
Stegmann, Alexander P. A.
Stumpel, Constance T. R. M.
Tanabe, Saori
Uctepe, Eyyup
Utine, G. Eda
Veenstra-Knol, Hermine E.
Venkateswaran, Sunita
Vilain, Catheline
Vincent-Delorme, Catherine
Vulto-van Silfhout, Anneke T.
Wheeler, Patricia
Wilson, Golder N.
Wilson, Louise C.
Wollnik, Bernd
Kosho, Tomoki
Wieczorek, Dagmar
Eichler, Evan
Pfundt, Rolph
de Vries, Bert B. A.
Clayton-Smith, Jill
Santen, Gijs W. E.

September 2019

The original version of this Article contained an error in the spelling of the author Pleuntje J. va...

Publisher correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways

Duffy, David L.
Zhu, Gu
Li, Xin
Sanna, Marianna
Iles, Mark M.
Jacobs, Leonie C.
Evans, David M.
Yazar, Seyhan
Beesley, Jonathan
Law, Matthew H.
Kraft, Peter
Visconti, Alessia
Taylor, John C.
Liu, Fan
Wright, Margaret J.
Henders, Anjali K.
Bowdler, Lisa
Glass, Dan
Ikram, M. Arfan
Uitterlinden, André G.
Madden, Pamela A.
Heath, Andrew C.
Nelson, Elliot C.
Green, Adele C.
Chanock, Stephen
Barrett, Jennifer H.
Brown, Matthew A.
Hayward, Nicholas K.
MacGregor, Stuart
Sturm, Richard A.
Hewitt, Alex W.

January 2019

The original version of this Article contained errors in the spelling of the authors Fan Liu and M. ...

Correction: Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability

Riazuddin, S.
Hussain, M.
Razzaq, A.
Iqbal, Z.
Shahzad, M.
Polla, D.L.
Song, Y.
van Beusekom, E.
Khan, A.A.
Tomas-Roca, L.
Rashid, M.
Zahoor, M.Y.
Wissink-Lindhout, W.M.
Basra, M.A.R.
Ansar, M.
Agha, Z.
van Heeswijk, K.
Rasheed, F.
Van de Vorst, M.
Veltman, J.A.
Gilissen, C.
Akram, J.
Kleefstra, T.
Assir, M.Z.
Grozeva, D.
Carss, K.
Raymond, F.L.
O'Connor, T.D.
Riazuddin, S.A.
Khan, S.N.
Ahmed, Z.M.
de Brouwer, A.P.M.
van Bokhoven, H.
UK10K, U.K.1.0.K.

November 2020

This Article was originally published under a CC BY-NC-SA 4.0 license, but has now been made availab...

Correction: Clinical and genetic characterization of chanarin-dorfman syndrome patients: first report of large deletions in the ABHD5 gene

Redaelli, Chiara
Coleman, Rosalind
Moro, Laura
Sertedaki, Amalia
Kakourou, Talia
Elsayed, Solaf
Prati, Daniele
Colli, Agostino
Mela, Donatella
Colombo, Roberto
Tavian, Daniela

February 2011

AbstractFollowing the publication of this article [Redaelli C et al, Clinical and genetic characteri...

Correction to: Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case report

Abstract

Extracted data

Correction to: Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case report

Abstract

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