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Recurrent mutations in the deafness geneGJB2 (connexin 26) in British Asian families

Authors

  1. Dr Bitner-Glindzicz, mbitnerg{at}ich.ucl.ac.uk
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Citation

Rickard S, Kelsell DP, Sirimana T, et al
Recurrent mutations in the deafness geneGJB2 (connexin 26) in British Asian families
Journal of Medical Genetics 2001;38:530-533.

Publication history

  • First published August 1, 2001.
Online issue publication 
April 27, 2016

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Journal of Medical Genetics