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...
Main Authors: | , , , , , , , , , , , , |
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Outros autores: | |
Formato: | Journal article |
Idioma: | English |
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Nature Publishing Group
2009
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