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<i>CYP1B1</i> mutational screening in a Portuguese cohort of primary congenital glaucoma patients

M. J. Simões (2820919)
S. Carmona (2820916)
R. Roberts (2820928)
G. Wainwright (2820925)
C. Faro (2820922)
E. Silva (2820934)
C. Egas (2820931)

Publication date

June 2016

DOI

10.6084/m9.figshare.3422833.v1

Abstract

<i>CYP1B1</i> mutational screening in a Portuguese cohort of primary congenital glaucoma patient

Extracted data

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Ivan M. Tavares (740055)
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Simone Finzi (740067)
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Ezequiel Campos-mollo
María-pilar López-garrido
Cristina Blanco-marchite
Julián Garcia-feijoo
Jesús Peralta
José Belmonte-martínez
Carmen Ayuso
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Badeeb, O.M.
Micheal, S.
Koenekoop, R.K.
Hollander, A.I. den
Hedrawi, M.T.

January 2014

BACKGROUND: CYP1B1 is the most commonly mutated gene in primary congenital glaucoma (PCG). This stud...

CYP1B1 mutation profile of Iranian primary congenital glaucoma patients and associated haplotypes

Chitsazian, F.
Tusi, B.K.
Elahi, E.
Saroei, H.A.
Sanati, M.H.
Yazdani, S.
Pakravan, M.
Nilforooshan, N.
Eslami, Y.
Zare Mehrjerdi, M.A.
Zareei, R.
Jabbarvand, M.
Abdolahi, A.
Lasheyee, A.R.
Etemadi, A.
Bayat, B.
Sadeghi, M.
Banoei, M.M.
Ghafarzadeh, B.
Rohani, M.R.
Rismanchian, A.
Thorstenson, Y.
Sarfarazi, M.

January 2007

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August 2016

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Dimasi, DP
Hewitt, AW
Straga, T
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Casey, T
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Craig, JE

January 2007

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Screening of CYP1B1 and LTBP2 genes in Saudi families with primary congenital glaucoma: Genotype-phenotype correlation

Michael A. Hauser
Saleh A. Al-obeidan

August 2016

Purpose: Primary congenital glaucoma (PCG) is a severe form of glaucoma that presents early in life....

Mutational Screening Of Cyp1B1 In Turkish Pcg Families And Functional Analyses Of Newly Detected Mutations

Bagiyeva, Sefayet
Marfany, Gemma
Gonzalez-Angulo, Olga
Gonzalez-Duarte, Roser

January 2007

Purpose: To investigate the genetic basis of primary congenital glaucoma (PCG) in a collection of Tu...

Mutations in CYP1B1, the Gene for Cytochrome P4501B1, Are the Predominant Cause of Primary Congenital Glaucoma in Saudi Arabia

Bejjani, Bassem A.
Lewis, Richard Alan
Tomey, Karim F.
Anderson, Kent L.
Dueker, David K.
Jabak, Monzer
Astle, William F.
Otterud, Brith
Leppert, Mark
Lupski, James R.

February 1998

SummaryThe autosomal recessive disorder primary congenital glaucoma (PCG) is caused by unknown devel...