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


No abstract provided

Bibliographic Information

Digital Object Identifier:

PubMed Identifier: 20346443

Publication URI:

Type: Journal Article/Review

Volume: 68

Parent Publication: Biological psychiatry

Issue: 4

ISSN: 0006-3223