Article info
PDFGenotype-phenotype correlations
Original article
Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes
- Correspondence to Dr Thomas B Friedman, Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, 5 Research Court, Rockville, MD 20850, USA; friedman{at}nidcd.nih.gov
Citation
Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes
Publication history
- Received June 14, 2011
- Revised August 10, 2011
- Accepted August 15, 2011
- First published September 22, 2011.
Online issue publication
April 27, 2016
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© 2011, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.