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A novel C202F mutation in the connexin26 gene (GJB2) associated with autosomal dominant isolated hearing loss

Authors

  1. Dr Morlé, l-morle{at}univ-lyon1.fr
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Citation

Morlé L, Bozon M, Alloisio N, et al
A novel C202F mutation in the connexin26 gene (GJB2) associated with autosomal dominant isolated hearing loss
Journal of Medical Genetics 2000;37:368-370.

Publication history

  • Revised October 15, 1999
  • Accepted October 18, 1999
  • First published May 1, 2000.
Online issue publication 
April 27, 2016

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Journal of Medical Genetics