MET and autism susceptibility: family and case–control studies

Autism is a common, severe and highly heritable neurodevelopmental disorder. The International Molecular Genetic Study of Autism Consortium (IMGSAC) genome screen for linkage in affected sib-pair families identified a chromosome 7q susceptibility locus (AUTS1), that has subsequently shown evidence o...

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Main Authors: Sousa, Inês, Clark, Taane G, Toma, Claudio, Kobayashi, Kazuhiro, Choma, Maja, Holt, Richard, Sykes, Nuala H, Lamb, Janine A, Bailey, Anthony J, Battaglia, Agatino, Maestrini, Elena, Monaco, Anthony P
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2009
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2685893/
https://ncbi.nlm.nih.gov/pubmed/19002214
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2008.215
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