Browsing Psychiatry (Scholarly Publications) by Subject ", PLD5, POU6F2, ST8SIA2 and TAF1C"
Now showing items 1-1 of 1
-
A genomewide scan for common alleles affecting risk for autism.
(Oxford University Press, 2010)Although autism spectrum disorders (ASDs) have a substantial genetic basis, most of the known genetic risk has been traced to rare variants, principally copy number variants (CNVs). To identify common risk variation, the ...