A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism-Reference-Cited by-同舟云学术

A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism

Published:2008-01 Issue:1 Volume:82 Page:160-164
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Arking Dan E.,Cutler David J.,Brune Camille W.,Teslovich Tanya M.,West Kristen,Ikeda Morna,Rea Alexis,Guy Moltu,Lin Shin,Cook Edwin H.,Chakravarti Aravinda

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference18 articles.

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4. Combining information from multiple sources in the diagnosis of autism spectrum disorders;Risi;J. Am. Acad. Child Adolesc. Psychiatry,2006

5. Undetected genotyping errors cause apparent overtransmission of common alleles in the transmission/disequilibrium test;Mitchell;Am. J. Hum. Genet.,2003

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