Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability.

Autism is a common neurodevelopmental disorder with a complex mode of inheritance. It is one of the most highly heritable of the complex disorders, although the underlying genetic factors remain largely unknown. Here, we report mutations in the X-chromosome PTCHD1 (patched-related) gene in seven fam...

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Bibliographic Details
Main Authors:	Noor, A, Whibley, A, Marshall, C, Gianakopoulos, P, Piton, A, Carson, A, Orlic-Milacic, M, Lionel, A, Sato, D, Pinto, D, Drmic, I, Noakes, C, Senman, L, Zhang, X, Mo, R, Gauthier, J, Crosbie, J, Pagnamenta, A, Munson, J, Estes, A, Fiebig, A, Franke, A, Schreiber, S, Stewart, A, Roberts, R
Format:	Journal article
Language:	English
Published:	2010

Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability.

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