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

Lookup NU author(s): Professor Jeremy ParrORCiD

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Publication metadata

Author(s): Pagnamenta AT, Bacchelli E, de Jonge MV, Mirza G, Scerri TS, Minopoli F, Chiocchetti A, Ludwig KU, Hoffmann P, Paracchini S, Lowy E, Harold DH, Chapman JA, Klauck SM, Poustka F, Houben RH, Staal WG, Ophoff RA, O'Donovan MC, Williams J, Northen MM, Schulte Korne G, Deloukas P, Ragoussis J, Bailey AJ, Maestrini E, Monaco AP, International Molecular Genetic Study Of Autism Consortium

Publication type: Article

Publication status: Published

Journal: Biological Psychiatry

Year: 2010

Volume: 68

Issue: 4

Pages: 320-328

Print publication date: 26/03/2010

ISSN (print): 0006-3223

ISSN (electronic): 1873-2402

Publisher: Elsevier Inc.

URL: http://dx.doi.org/10.1016/j.biopsych.2010.02.002

DOI: 10.1016/j.biopsych.2010.02.002

PubMed id: 20346443

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