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Loss-of-Function Mutations in the PRPS1 Gene Cause a Type of Nonsyndromic X-linked Sensorineural Deafness, DFN2

✍ Scribed by Xuezhong Liu; Dongyi Han; Jianzhong Li; Bing Han; Xiaomei Ouyang; Jing Cheng; Xu Li; Zhanguo Jin; Youqin Wang; Maria Bitner-Glindzicz; Xiangyin Kong; Heng Xu; Albena Kantardzhieva; Roland D. Eavey; Christine E. Seidman; Jonathan G. Seidman; Li L. Du; Zheng-Yi Chen; Pu Dai; Maikun Teng; Denise Yan; Huijun Yuan

Book ID: 113422741
Publisher: American Society of Human Genetics
Year: 2010
Tongue: English
Weight: 1014 KB
Volume: 86
Category: Article
ISSN: 0002-9297
DOI: 10.1016/j.ajhg.2009.11.015

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