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

Published December 21, 2012 in PubMed

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

http://www.ncbi.nlm.nih.gov/pubmed/23160955

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