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                                       Details for article 9 of 15 found articles
 
 
  Loss-of-Function Mutations in the PRPS1 Gene Cause a Type of Nonsyndromic X-linked Sensorineural Deafness, DFN2
 
 
Title: Loss-of-Function Mutations in the PRPS1 Gene Cause a Type of Nonsyndromic X-linked Sensorineural Deafness, DFN2
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
Appeared in: The American journal of human genetics
Paging: Volume 86 (2010) nr. 1 pages 7 p.
Year: 2010
Contents:
Publisher: The American Society of Human Genetics
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 9 of 15 found articles
 
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 Koninklijke Bibliotheek - National Library of the Netherlands