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Original article
A common founder for the 35delG GJB2gene mutation in connexin 26 hearing impairment

Authors

  1. Professor Van Camp,gvcamp{at}uia.ua.ac.be
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Citation

Van Laer L, Coucke P, Mueller RF, et al
A common founder for the 35delG GJB2gene mutation in connexin 26 hearing impairment
Journal of Medical Genetics 2001;38:515-518.

Publication history

  • Revised April 26, 2001
  • Accepted May 3, 2001
  • First published August 1, 2001.
Online issue publication 
April 27, 2016

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Journal of Medical Genetics