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                                       Details for article 10 of 20 found articles
 
 
  Molecular Basis of DFNB73: Mutations of BSND Can Cause Nonsyndromic Deafness or Bartter Syndrome
 
 
Title: Molecular Basis of DFNB73: Mutations of BSND Can Cause Nonsyndromic Deafness or Bartter Syndrome
Author: Riazuddin, Saima
Anwar, Saima
Fischer, Martin
Ahmed, Zubair M.
Khan, Shahid Y.
Janssen, Audrey G.H.
Zafar, Ahmad U.
Scholl, Ute
Husnain, Tayyab
Belyantseva, Inna A.
Friedman, Penelope L.
Riazuddin, Sheikh
Friedman, Thomas B.
Fahlke, Christoph
Appeared in: The American journal of human genetics
Paging: Volume 85 (2009) nr. 2 pages 8 p.
Year: 2009
Contents:
Publisher: The American Society of Human Genetics
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 10 of 20 found articles
 
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