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A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing loss

Authors

  1. Correspondence to Dr Sadaf Naz, School of Biological Sciences, University of the Punjab, Lahore 54590, Pakistan; naz.sbs{at}pu.edu.pk
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Citation

Mujtaba G, Schultz JM, Imtiaz A, et al
A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing loss
Journal of Medical Genetics 2015;52:548-552.

Publication history

  • Received January 16, 2015
  • Revised March 3, 2015
  • Accepted April 15, 2015
  • First published May 4, 2015.
Online issue publication 
April 27, 2016

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