The worldwide frequency of MYO15A gene mutations in patients with 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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Bibliografiske detaljer
Udgivet i:Iran J Basic Med Sci
Main Authors: Farjami, Mahsa, Assadi, Reza, Afzal Javan, Fahimeh, Alimardani, Malihe, Eslami, Saeid, Mansoori Derakhshan, Sima, Eslahi, Atieh, Mojarrad, Majid
Format: Artigo
Sprog:Inglês
Udgivet: Mashhad University of Medical Sciences 2020
Fag:
Review Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7395192/
https://ncbi.nlm.nih.gov/pubmed/32774803
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.22038/IJBMS.2020.35977.8563
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