Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia. (2010)

First Author: Pagnamenta AT
Attributed to:  The Autism Genome Project funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.biopsych.2010.02.002

PubMed Identifier: 20346443

Publication URI: http://europepmc.org/abstract/MED/20346443

Type: Journal Article/Review

Volume: 68

Parent Publication: Biological psychiatry

Issue: 4

ISSN: 0006-3223