Diverse pattern of gap junction beta-2 and gap junction beta-4 genes mutations and lack of contribution of DFNB21, DFNB24, DFNB29, and DFNB42 loci in autosomal recessive nonsyndromic hearing loss patients in Hormozgan, Iran

BACKGROUND: We aimed to determine the contribution of four DFNB loci and mutation analysis of gap junction beta-2 (GJB2) and GJB4 genes in autosomal recessive nonsyndromic hearing loss (ARNSHL) in South of Iran. MATERIALS AND METHODS: A total of 36 large ARNSHL pedigrees with at least two affected s...

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Publicado en:J Res Med Sci
Autores principales: Laleh, Masoud Akbarzadeh, Naseri, Marzieh, Zonouzi, Ali Akbar Poursadegh, Zonouzi, Ahmad Poursadegh, Masoudi, Marjan, Ahangari, Najmeh, Shams, Leila, Nejatizadeh, Azim
Formato: Artigo
Lenguaje:Inglês
Publicado: Medknow Publications & Media Pvt Ltd 2017
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Original Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC5583625/
https://ncbi.nlm.nih.gov/pubmed/28900455
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/jrms.JRMS_976_16
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