Screening of 10 DFNB Loci Causing Autosomal Recessive Non-Syndromic Hearing Loss in Two Iranian Populations Negative for GJB2 Mutations

BACKGROUND: Autosomal recessive non-syndromic hearing loss (ARNSHL), one of the global public health concerns, is marked by a high degree of genetic heterogeneity. The role of GJB2, as the most common cause of ARNSHL, is only <20% in the Iranian population. Here, we aimed to determine the relativ...

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Detalles Bibliográficos
Autores principales: KOOHIYAN, Mahbobeh, REIISI, Somayeh, AZADEGAN-DEHKORDI, Fatemeh, SALEHI, Mansoor, ABTAHI, Hamidreza, HASHEMZADEH-CHALESHTORI, Morteza, NOORI-DALOII, Mohammad Reza, TABATABAIEFAR, Mohammad Amin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2019
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6825662/
https://www.ncbi.nlm.nih.gov/pubmed/31700827

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6825662/
https://www.ncbi.nlm.nih.gov/pubmed/31700827

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