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

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


Book ID
116195573
Publisher
American Society of Human Genetics
Year
2008
Tongue
English
Weight
481 KB
Volume
82
Category
Article
ISSN
0002-9297

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## Abstract Cutaneous malignant melanoma (CMM) is an etiologically heterogeneous disease with genetic, environmental (sun exposure) and host (pigmentation/nevi) factors and their interactions contributing to risk. Genetic variants in DNA repair genes may be particularly important since their altere