Clinical evidence for dystrophin dysfunction as a cause of hearing loss in locus DFN4
Author:
Publisher
Wiley
Subject
Otorhinolaryngology
Reference21 articles.
1. Van Camp G, Smith RJH. Hereditary hearing loss homepage. World Wide Web URL: http:dnalabwww.uia.ac.be/dnalab/hhh, 1998.
2. Mutations in the myosin VIIA gene cause nonsyndromic recessive deafness;Liu;Nature Genet,1997
3. Autosomal dominant nonsyndromic deafness (DFNA11) caused by a mutation in the myosin VIIA gene;Liu;Nature Genet,1997
4. Nonsyndromic deafness DFNA1 associated with mutation of the human homolog HDIA1 of the Drosophila diaphanous gene;Lynch;Science,1997
5. Association of unconventional myosin MYO15 mutations with human nonsyndromic DFNB3;Wang;Science,1998
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