Publications:

A family with autism and rare copy number variants disrupting the Duchenne/Becker muscular dystrophy gene DMD and TRPM3.

Journal Of Neurodevelopmental Disorders

Pagnamenta, Alistair T AT; Holt, Richard R; Yusuf, Mohammed M; Pinto, Dalila D; Wing, Kirsty K; Betancur, Catalina C; Scherer, Stephen W SW; Volpi, Emanuela V EV; Monaco, Anthony P AP

Publication Date: 2011-06

Variant appearance in text: rs1795588

PubMed Link: 21484199

Variant Present in the following documents:

• Main text

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