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Updated: Mar 23, 2026

A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia
Published on: June 15, 2011
Novel germline ERCC5 mutations identified in a xeroderma pigmentosum complementation group G pedigree
Tao Wang1, Chen-Chen Xu1, Xi-Ping Zhou1
1Department of Dermatology, Peking Union Medical College Hospital, Peking Union Medical College & Chinese Academy of Medical Sciences, Beijing, China.
No abstract available in PubMed .
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