Loss-of-Function Mutations in the PRPS1 Gene Cause a Type of Nonsyndromic X-linked Sensorineural Deafness, DFN2-Reference-Cited by-同舟云学术

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

Published:2010-01 Issue:1 Volume:86 Page:65-71
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

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

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference19 articles.

1. Sex linked deafness: Wilde revisited;Reardon;J. Med. Genet.,1990

2. Epidemiology, etiology, and genetic patterns;Cohen,1995

3. Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4;de Kok;Science,1995

4. Mapping of DFN2 to Xq22;Tyson;Hum. Mol. Genet.,1996

5. Hereditary postlingual sensorineural hearing loss mapping to chromosome Xq21;Manolis;Am. J. Otol.,1999

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