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...

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Main Authors: 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
格式: Artigo
語言:Inglês
出版: The American Society of Human Genetics 2004
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC1182268/
https://ncbi.nlm.nih.gov/pubmed/14963808
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