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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Detalles Bibliográficos
Autores principales: Farjami, Mahsa, Assadi, Reza, Afzal Javan, Fahimeh, Alimardani, Malihe, Eslami, Saeid, Mansoori Derakhshan, Sima, Eslahi, Atieh, Mojarrad, Majid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2020
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7395192/
https://www.ncbi.nlm.nih.gov/pubmed/32774803
http://dx.doi.org/10.22038/IJBMS.2020.35977.8563

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7395192/
https://www.ncbi.nlm.nih.gov/pubmed/32774803
http://dx.doi.org/10.22038/IJBMS.2020.35977.8563

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