Mutation Detection in MYO15A Gene in an Iranian Family with Non-Syndromic Hearing Loss

Mutation Detection in MYO15A Gene in an Iranian Family with Non-Syndromic Hearing Loss

Hearing loss, recognized as one of the most prevalent sensory disorders, encompasses both syndromic and non-syndromic manifestations, with the identification of 87 genes and over 100 genetic loci in autosomal recessive non-syndromic hearing loss marking significant progress in understanding its gene...

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Bibliographic Details
Main Authors: Mostafa Neissi, Misagh Mohammadi-Asl, Mojdeh Roghani, Adnan Issa Al-Badran, Javad Mohammadi-Asl
Format: Article
Language:English
Published: International Medical Research and Development Corporation 2024-03-01
Series:International Journal of Biomedicine
Subjects:
hearing loss
myo15a gene
mutation
Online Access:http://www.ijbm.org/articles/i53/ijbm_14(1)_cr3.pdf

Internet

http://www.ijbm.org/articles/i53/ijbm_14(1)_cr3.pdf

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