Condition: Deafness, Autosomal Recessive 3


rs117071200 in LOC105371566;MYO15A gene and Deafness, Autosomal Recessive 3 PMID 23967202 2013 Targeted exon sequencing successfully discovers rare causative genes and clarifies the molecular epidemiology of Japanese deafness patients.

PMID 25792667 2015 Mutations in the MYO15A gene are a significant cause of nonsyndromic hearing loss: massively parallel DNA sequencing-based analysis.

PMID 9603736 1998 Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.

PMID 11735029 2001 Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome.

PMID 24926664 2014 Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafness.

PMID 23767834 2013 Genetic etiology study of the non-syndromic deafness in Chinese Hans by targeted next-generation sequencing.

PMID 27870113 2016 Targeted Resequencing of Deafness Genes Reveals a Founder MYO15A Variant in Northeastern Brazil.

PMID 20642360 2010 Recurrent and private MYO15A mutations are associated with deafness in the Turkish population.

PMID 23208854 2013 A sensitive and specific diagnostic test for hearing loss using a microdroplet PCR-based approach and next generation sequencing.

PMID 24875298 2014 Targeted next-generation sequencing of deafness genes in hearing-impaired individuals uncovers informative mutations.

PMID 24123792 2013 A post-hoc comparison of the utility of sanger sequencing and exome sequencing for the diagnosis of heterogeneous diseases.

PMID 30828794 2019 Exome sequencing reveals novel variants and unique allelic spectrum for hearing impairment in Filipino cochlear implantees.

PMID 17546645 2007 Mutational spectrum of MYO15A: the large N-terminal extension of myosin XVA is required for hearing.

rs121908965 in MYO15A;LOC105371566 gene and Deafness, Autosomal Recessive 3 PMID 9603736 1998 Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.

PMID 24926664 2014 Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafness.

PMID 11735029 2001 Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome.

PMID 27734841 2017 A novel founder MYO15A frameshift duplication is the major cause of genetic hearing loss in Oman.

PMID 22736430 2012 Screening for MYO15A gene mutations in autosomal recessive nonsyndromic, GJB2 negative Iranian deaf population.

rs121908969 in MYO15A;LOC105371566;LOC105371567 gene and Deafness, Autosomal Recessive 3 PMID 24926664 2014 Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafness.

PMID 11735029 2001 Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome.

PMID 9603736 1998 Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.

PMID 21917145 2011 Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in Middle Eastern families.

PMID 23767834 2013 Genetic etiology study of the non-syndromic deafness in Chinese Hans by targeted next-generation sequencing.