Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.

Source: 
PubMed
Date Published: 
December 21, 2012
Abstract: 

Data supports associations between specific genes and reciprocal subphenotypes (CHD8-macrocephaly and DYRK1A-microcephaly) and replicate the importance of a β-catenin-chromatin-remodeling network to ASD etiology.