Common genetic variants on 1p13.2 associate with risk of autism
Autism is a highly heritable neurodevelopmental disorder, and known genetic variants, mostly rare, account only for a small proportion of cases. Here we report a genome-wide association study on autism using two Chinese cohorts as gene discovery ( n =2150) and three data sets of European ancestry po...
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Published in | Molecular psychiatry Vol. 19; no. 11; pp. 1212 - 1219 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
01.11.2014
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
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