Results 101 to 109 of about 334 (109)
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Mutational Spectrum ofMYO15Aand the Molecular Mechanisms of DFNB3 Human Deafness

Human Mutation, 2016
Jonathan Bird   +2 more
exaly  

Report of a Novel Splicing Mutation in the MYO15A Gene in a Patient With Sensorineural Hearing Loss and Spectrum of the MYO15A Mutations

Clinical Medicine Insights: Case Reports, 2019
Elinaz Akbariazar   +2 more
exaly  

Screening for MYO15A gene mutations in autosomal recessive nonsyndromic, GJB2 negative Iranian deaf population

American Journal of Medical Genetics, Part A, 2012
Fatemehsadat Esteghamat   +2 more
exaly  

Mutations in the MYO15A Gene Are a Significant Cause of Nonsyndromic Hearing Loss

Annals of Otology, Rhinology and Laryngology, 2015
Shin-Ya Nishio   +2 more
exaly  

Whole exome sequencing identifies novel compound heterozygous pathogenic variants in the MYO15A gene leading to autosomal recessive non-syndromic hearing loss

Molecular Biology Reports, 2020
Hamidreza Abtahi   +2 more
exaly  

Mutations in the first MyTH4 domain of MYO15A are a common cause of DFNB3 hearing loss

Laryngoscope, 2009
Melanie Bahlo   +2 more
exaly  

Recurrent and Private MYO15A Mutations Are Associated with Deafness in the Turkish Population

Genetic Testing and Molecular Biomarkers, 2010
Duygu Duman   +2 more
exaly  

Screening of the DFNB3 Locus: Identification of Three Novel Mutations of MYO15A Associated with Hearing Loss and Further Suggestion for Two Distinctive Genes on This Locus

Genetic Testing and Molecular Biomarkers, 2009
Masmoudi Saber   +2 more
exaly  

Computational study of the potential impact of WHRN protein missense SNPs on WHRN-MYO15A protein complex interaction and their association with Usher syndrome

Journal of Biomolecular Structure and Dynamics
exaly  
medicine
hearing loss
deafness
non-syndromic hearing loss
biological psychiatry
neurosciences
neuropsychiatry
dfnb3
mutation
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