Screening for MYO15A Gene Mutations in Autosomal Recessive Nonsyndromic, GJB2 Negative Iranian Deaf Population

MYO15A is located at the DFNB3 locus on chromosome 17p11.2, and encodes myosin-XV, an unconventional myosin critical for the formation of stereocilia in hair cells of cochlea. Recessive mutations in this gene lead to profound autosomal recessive nonsyndromic hearing loss (ARNSHL) in humans and the s...

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Main Authors: Fattahi, Zohreh, Shearer, A. Eliot, Babanejad, Mojgan, Bazazzadegan, Niloofar, Almadani, Seyed Navid, Nikzat, Nooshin, Jalalvand, Khadijeh, Arzhangi, Sanaz, Esteghamat, Fatemehsadat, Abtahi, Rezvan, Azadeh, Batool, Smith, Richard J.H., Kahrizi, Kimia, Najmabadi, Hossein
Formato: Artigo
Idioma:Inglês
Publicado em: 2012
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3757123/
https://ncbi.nlm.nih.gov/pubmed/22736430
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.34411
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