Original paper
Replication of a rare risk haplotype on 1p36.33 for autism spectrum disorder
Abstract
Hundreds of genes have been implicated in autism spectrum disorders (ASDs). In genetically heterogeneous conditions, large families with multiple affected individuals provide strong evidence implicating a rare variant, and replication of the same variant in multiple families is unusual. We previously published linkage analyses and follow-up exome sequencing in seven large families with ASDs, implicating 14 rare exome variants. These included...
Paper Details
Title
Replication of a rare risk haplotype on 1p36.33 for autism spectrum disorder
Published Date
Oct 1, 2018
Journal
Volume
137
Issue
10
Pages
807 - 815
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Notes
History