Novel mutations in MYTH4-FERM domains of myosin 15 are associated with autosomal recessive nonsyndromic hearing loss
Author:
Publisher
Elsevier BV
Subject
Otorhinolaryngology,General Medicine,Pediatrics, Perinatology and Child Health
Reference78 articles.
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2. Mutations in the MYO15A gene are a significant cause of nonsyndromic hearing loss: massively parallel DNA sequencing-based analysis;Miyagawa;Ann. Otol. Rhinol. Laryngol.,2015
3. Genetic etiology study of the non-syndromic deafness in Chinese Hans by targeted next-generation sequencing;Yang;Orphanet J. Rare Dis.,2013
4. Mutations in the first MyTH4 domain of MYO15A are a common cause of DFNB3 hearing loss;Shearer;Laryngoscope,2009
5. A comprehensive study to determine heterogeneity of autosomal recessive nonsyndromic hearing loss in Iran;Babanejad;Am. J. Med. Genet.,2012
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1. Analysis of the genotype–phenotype correlation of MYO15A variants in Chinese non-syndromic hearing loss patients;BMC Medical Genomics;2022-03-26
2. Novel Cellular Stress Models with Implications in Understanding and Treating ENT Pathologies;Biomedical Translational Research;2022
3. Whole-Exome Sequencing Identifies a Recurrent Small In-Frame Deletion in MYO15A Causing Autosomal Recessive Nonsyndromic Hearing Loss in 3 Iranian Pedigrees;Laboratory Medicine;2021-08-13
4. Heterogeneity of MYO15A variants significantly determine the feasibility of acoustic stimulation with hearing aid and cochlear implant;Hearing Research;2021-05
5. Novel MYO15A variants are associated with hearing loss in the two Iranian pedigrees;BMC Medical Genetics;2020-11-18
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