Zobrazeno 1 - 2 of 2 pro vyhledávání: '"Masoud AKBARZADEHLALEH"'
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Akademický článek
Genetic Linkage Analysis of DFNB4, DFNB28, DFNB93 Loci in Autosomal Recessive Non-syndromic Hearing Loss: Evidence for Digenic Inheritance in GJB2 and GJB3 Mutations
Autor: Marzieh NASERI, Masoud AKBARZADEHLALEH, Marjan MASOUDI, Najmeh AHANGARI, Ali Akbar POURSADEGH ZONOUZI, Ahmad POURSADEGH ZONOUZI, Leila SHAMS, Azim NEJATIZADEH
Publikováno v: Iranian Journal of Public Health, Vol 47, Iss 1 (2017)
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
Externí odkaz: https://doaj.org/article/c43595458d784b69b61d684b565be462
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2
Genetic Linkage Analysis of DFNB4, DFNB28, DFNB93 Loci in Autosomal Recessive Non-syndromic Hearing Loss: Evidence for Digenic Inheritance in
Autor: Marzieh, Naseri, Masoud, Akbarzadehlaleh, Marjan, Masoudi, Najmeh, Ahangari, Ali Akbar, Poursadegh Zonouzi, Ahmad, Poursadegh Zonouzi, Leila, Shams, Azim, Nejatizadeh
Publikováno v: Iranian Journal of Public Health
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
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::25f80fbf3c1d57206b16dd29048f2cf8
https://pubmed.ncbi.nlm.nih.gov/29318123
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Plný text Recenzováno Digitální knihovna AV ČR
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