Characterization of a Family with Rare Deletions in CNTNAP5 and DOCK4 Suggests Novel Risk Loci for Autism and Dyslexia
BACKGROUND: Autism spectrum disorders (ASDs) are characterized by social, communication, and behavioral deficits and complex genetic etiology. A recent study of 517 ASD families implicated DOCK4 by single nucleotide polymorphism (SNP) association and a microdeletion in an affected sibling pair. METH...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Elsevier
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2941017/ https://www.ncbi.nlm.nih.gov/pubmed/20346443 http://dx.doi.org/10.1016/j.biopsych.2010.02.002 |