FOXP1-related intellectual disability syndrome: a recognisable entity
- Meerschaut, Ilse
- Rochefort, Daniel
- Revençu, Nicole
- Pètre, Justine
- Corsello, Christina
- Rouleau, Guy A
- Hamdan, Fadi F
- Michaud, Jacques L
- Morton, Jenny
- Radley, Jessica
- Ragge, Nicola
- García-Miñaúr, Sixto
- Lapunzina, Pablo
- Bralo, Maria Palomares
- Mori, Maria Ángeles
- Moortgat, Stéphanie
- Benoit, Valérie
- Mary, Sandrine
- Bockaert, Nele
- Oostra, Ann
- Vanakker, Olivier
- Velinov, Milen
- de Ravel de l'Argentière, Thomy
- Mekahli, Djalila
- Sebat, Jonathan
- Vaux, Keith K
- DiDonato, Nataliya
- Hanson-Kahn, Andrea K
- Hudgins, Louanne
- Dallapiccola, Bruno
- Novelli, Antonio
- Tarani, Luigi
- Andrieux, Joris
- Parker, Michael J
- Neas, Katherine
- Ceulemans, Berten
- Schoonjans, An-Sofie
- Prchalova, Darina
- Havlovicova, Marketa
- Hancarova, Miroslava
- Budisteanu, Magdalena
- Dheedene, Annelies
- Menten, Björn
- Dion, Patrick A
- Lederer, Damien
- Callewaert, Bert
Publication date
September 2017
DOI Publisher
BMJ Journal
Journal of Medical GeneticsAbstract
Mutations in forkhead box protein P1 (FOXP1) cause intellectual disability (ID) and specific language impairment (SLI), with or without autistic features (MIM: 613670). Despite multiple case reports no specific phenotype emerged so far.status: publishe
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