Rare heterozygous truncating variations and risk of autism spectrum disorder: Whole‐exome sequencing of a multiplex family and follow‐up study in a Japanese population

Publisher： John Wiley & Sons Inc

E-ISSN： 1440-1819|69|8|472-476

ISSN： 1323-1316

Source： PSYCHIATRY AND CLINICAL NEUROSCIENCES, Vol.69, Iss.8, 2015-08, pp. : 472-476

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