Skip to main content
Rare deleterious mutations of the gene EFR3A in autism spectrum disorders
Published Web Location
http://europepmc.org/articles/PMC4032628?pdf=renderNo data is associated with this publication.
Abstract
Background: Whole-exome sequencing studies in autism spectrum disorder (ASD) have identified de novo mutations in novel candidate genes, including the synaptic gene Eighty-five Requiring 3A (EFR3A). EFR3A is a critical component of a protein complex requir
Many UC-authored scholarly publications are freely available on this site because of the UC's open access policies. Let us know how this access is important for you.