MET and autism susceptibility: family and case-control studies

Austism 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 7 q susceptibility locus (AUTS1), that has subsequently shown evidence...

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Detalles Bibliográficos
Main Authors: Sousa, I, Clark, T, Toma, C, Kobayashi, K, Choma, M, Holt, R, Sykes, N, Lamb, J, Bailey, A, Battaglia, A, Maestrini, E, Monaco, A, International Molecular Genetic Study of Autism Consortium (IMGSAC)
Outros autores: European Society of Human Genetics
Formato: Journal article
Idioma:English
Publicado: Nature Publishing Group 2009
Subjects: