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MYO15A gene
Known as:
MYO15A
, Myosin XVA Gene
, MYO15
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This gene plays a role in the structure of stereocilia.
National Institutes of Health
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Related topics
Related topics
6 relations
Cell Movement
Cytokinesis
Hearing
MYO15A protein, human
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
The prevalence of deafness-associated mutations in neonates: A meta-analysis of clinical trials.
Shuilian Chen
,
Zhijiang Liang
,
+6 authors
Qingguo Zhao
International Journal of Pediatric…
2019
Corpus ID: 81978360
2019
2019
Report of a Novel Splicing Mutation in the MYO15A Gene in a Patient With Sensorineural Hearing Loss and Spectrum of the MYO15A Mutations
E. Akbariazar
,
Ali Vahabi
,
Isa Abdi Rad
Clinical Medicine Insights: Case Reports
2019
Corpus ID: 203637960
Introduction: Autosomal recessive non-syndromic hearing loss (ARNSHL) is a genetically heterogeneous sensorineural disorder with…
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2018
2018
Spectrum of MYO15A mutations and report of a novel splicing mutation in an Iranian family with sensorineural hearing loss
pIsa Abdi Rad Elinaz AkbariAzar
,
Ali Vahabip
2018
Corpus ID: 116893329
2018
2018
Moleculargenetic Analyse of non-syndromic hearing-impairment in early childhood using the example of the gene MYO15 A
V. Arturi
,
A. Aschendorff
,
S. Arndt
,
R. Birkenhäger
,
R. Laszig
Laryngo-Rhino-Otologie
2018
Corpus ID: 81772405
Review
2017
Review
2017
Genetics Of Human Hereditary Hearing Impairment.
Rahat Meena
,
M. Ayub
Journal of Ayub Medical College
2017
Corpus ID: 11942004
Hereditary hearing impairment is heterogeneous type of disorder which can be caused due to environmental as well as genetical…
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2016
2016
Deafness genes in families with non-syndromic hearing loss in Shandong, China: a genetic study
X. Bai
,
Lei Xu
,
Fengguo Zhang
,
Yun Xiao
,
Jian-feng Li
,
Haibo Wang
The Lancet
2016
Corpus ID: 5586227
Review
2013
Review
2013
Author's response to reviews Title: Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families Authors:
U. Kim
2013
Corpus ID: 1156108
Title: Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean…
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2010
2010
Molecular Genetics of Deafness: The Roles of MYO15 and Thyroid Hormone.
Qi Fang
2010
Corpus ID: 81551323
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2004
2004
Cloning and chromosomal localization of MYO15A to chromosome 5 of the dog (Canis familiaris)
S. Rak
,
C. Drögemüller
,
+4 authors
O. Distl
Chromosome Research
2004
Corpus ID: 27503471
Mutations in the myosin XVA gene (MYO15A) cause congenital non-syndromic deafness in humans and mice. Therefore, the MYO15A gene…
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2002
2002
Localization of myosin XVA in endocrine tumors of gut and pancreas
S. La Rosa
,
C. Capella
,
R. Lloyd
Endocrine pathology
2002
Corpus ID: 20356974
The myosin superfamily includes conventional and unconventional myosin proteins. Among unconventional myosins, myosin XVA has…
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