The worldwide frequency of MYO15A gene mutations in patients with autosomal recessive non-syndromic hearing loss: A meta‐analysis

The worldwide frequency of MYO15A gene mutations in patients with autosomal recessive non-syndromic hearing loss: A meta‐analysis

MYO15A is the third most crucial gene in hereditary sensorineural hearing loss after GJB2 and SLC26A4. In the present study, we reviewed the prevalence of MYO15A mutations in patients with autosomal recessive non-syndromic hearing loss (ARNSHL). In this meta-analysis, we conducted a search of PubMed...

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Bibliographic Details
Main Authors:	Mahsa Farjami, Reza Asadi, Fahimeh Afzal Javan, Malihe Alimardani, Saeed Eslami, Sima Mansoori Derakhshan, Atieh Eslahi, Majid Mojarad
Format:	Article
Language:	English
Published:	Mashhad University of Medical Sciences 2020-07-01
Series:	Iranian Journal of Basic Medical Sciences
Subjects:	autosomal recessive deafness meta-analysis mutation myo15a non-syndromic hearing loss prevalence
Online Access:	http://ijbms.mums.ac.ir/article_15655_57e2e4a2ae3f2d97d5498723ad6da6b4.pdf

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