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Genetic Linkage Analysis of DFNB4, DFNB28, DFNB93 Loci in Autosomal Recessive Non-syndromic Hearing Loss: Evidence for Digenic Inheritance in GJB2 and GJB3 Mutations

BACKGROUND: Autosomal recessive non-syndromic hearing loss (ARNSHL) a most frequent hereditary type of hearing impairment, exhibit tremendous genetic heterogeneity. We aimed to determine the contribution of three common DFNB loci (DFNB4, DFNB28, and DFNB93), and mutation analysis of Gap Junction Bet...

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Publicat a:Iran J Public Health
Autors principals: NASERI, Marzieh, AKBARZADEHLALEH, Masoud, MASOUDI, Marjan, AHANGARI, Najmeh, POURSADEGH ZONOUZI, Ali Akbar, POURSADEGH ZONOUZI, Ahmad, SHAMS, Leila, NEJATIZADEH, Azim
Format: Artigo
Idioma:Inglês
Publicat: Tehran University of Medical Sciences 2018
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5756606/
https://ncbi.nlm.nih.gov/pubmed/29318123
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