Heterogeneity of MYO15A variants significantly determine the feasibility of acoustic stimulation with hearing aid and cochlear implant
Author:
Funder
National Research Foundation of Korea
Publisher
Elsevier BV
Subject
Sensory Systems
Reference39 articles.
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3. Identification of novel variants in MYO15A, OTOF, and RDX with hearing loss by next-generation sequencing;Bai;Mol. Genet. Genomic. Med.,2019
4. Prioritized sequencing of the second exon of MYO15A reveals a new mutation segregating in a Pakistani family with moderate to severe hearing loss;Bashir;Eur. J. Med. Genet.,2012
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Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Implementing next-generation sequencing for diagnosis and management of hereditary hearing impairment: a comprehensive review;Expert Review of Molecular Diagnostics;2024-08-28
2. Identification of novel compound heterozygous mutations of the MYO15A gene with autosomal recessive non‐syndromic hearing loss;Journal of Clinical Laboratory Analysis;2022-08-10
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