Characterization of a Family with Rare Deletions in CNTNAP5 and DOCK4 Suggests Novel Risk Loci for Autism and Dyslexia
Open Access
- 29 March 2010
- journal article
- research article
- Published by Elsevier in Biological Psychiatry
- Vol. 68 (4) , 320-328
- https://doi.org/10.1016/j.biopsych.2010.02.002
Abstract
No abstract availableKeywords
Funding Information
- Nancy Lurie Marks Family Foundation
- Simons Foundation
- Wellcome Trust (075491/Z/04)
- Deutsche Forschungsgemeinschaft
- European Union in the Sixth Framework Program
- LifeScienceHealth
- Dyslexia genes and neurobiological pathways
- National Institute of Mental Health
- United Kingdom Medical Research Council (G0000934)
- Wellcome Trust (068545/Z/02)
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