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Mutations of human TMHS cause recessively inherited non-syndromic hearing loss
  1. Correspondence to:
 Professor Sheikh Riazuddin
 National Centre of Excellence in Molecular Biology, University of the Punjab, 87 West Canal Bank Road, Thokar Niaz Baig, Lahore 53700, Pakistan; riaz{at}lhr.comsats.net.pk
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Citation

Shabbir MI, Ahmed ZM, Khan SY, et al
Mutations of human TMHS cause recessively inherited non-syndromic hearing loss

Publication history

  • Received November 24, 2005
  • Accepted January 24, 2006
  • Revised January 19, 2006
  • First published February 3, 2006.
Online issue publication 
April 27, 2016

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