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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Main Authors: Shearer, A. Eliot, Hildebrand, Michael S., Webster, Jennifer A., Kahrizi, Kimia, Jalalvand, Khadijeh, Arzhanginy, Sanaz, Kimberling, William J., Stephan, Dietrich, Bahlo, Melanie, Smith, Richard J.H., Najmabadi, Hossein
Formato: Artigo
Idioma:Inglês
Publicado em: 2009
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Article
Acesso em linha: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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