X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family

A large French family including members affected by nonspecific X-linked mental retardation, with or without autism or pervasive developmental disorder in affected male patients, has been found to have a 2–base-pair deletion in the Neuroligin 4 gene (NLGN4) located at Xp22.33. This mutation leads to...

Szczegółowa specyfikacja

Zapisane w:
Opis bibliograficzny
Główni autorzy: Laumonnier, Frédéric, Bonnet-Brilhault, Frédérique, Gomot, Marie, Blanc, Romuald, David, Albert, Moizard, Marie-Pierre, Raynaud, Martine, Ronce, Nathalie, Lemonnier, Eric, Calvas, Patrick, Laudier, Béatrice, Chelly, Jamel, Fryns, Jean-Pierre, Ropers, Hans-Hilger, Hamel, Ben C. J., Andres, Christian, Barthélémy, Catherine, Moraine, Claude, Briault, Sylvain
Format: Artigo
Język:Inglês
Wydane: The American Society of Human Genetics 2004
Hasła przedmiotowe:
Report
Dostęp online:https://ncbi.nlm.nih.gov/pmc/articles/PMC1182268/
https://ncbi.nlm.nih.gov/pubmed/14963808
Etykiety: Dodaj etykietę
Nie ma etykietki, Dołącz pierwszą etykiete!

Podobne zapisy