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Mutations in the MyTH4 domain of MYO15A are a common cause of DFNB3 hearing loss
OBJECTIVES: To use clinical and genetic analyses to determine the mutation causing autosomal recessive non-syndromic hearing loss (ARNSHL) segregating in two consanguineous Iranian families. STUDY DESIGN: Family study. METHODS: Members of each family received otologic and audiometric examination for...
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Autori principali: | , , , , , , , , , , |
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Natura: | Artigo |
Lingua: | Inglês |
Pubblicazione: |
2009
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Soggetti: | |
Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2885251/ https://ncbi.nlm.nih.gov/pubmed/19274735 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/lary.20116 |
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