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A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia
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NOD2/CARD15 gene mutation identified in a Chinese family with Blau syndrome

Haotian Xiang1, Ting Zhang, Mengping Chen

  • 1Ophthalmic Laboratories & Department of Ophthalmology, Translational Neuroscience Center, West China Hospital, Sichuan University, Chengdu, PR China.

Molecular Vision
|April 18, 2012
PubMed
Abstract

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