Skip to search formSkip to main contentSkip to account menu

MYO15A gene

Known as: MYO15A, Myosin XVA Gene, MYO15 
This gene plays a role in the structure of stereocilia.
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Introduction: Autosomal recessive non-syndromic hearing loss (ARNSHL) is a genetically heterogeneous sensorineural disorder with… 
Review
2017
Review
2017
Hereditary hearing impairment is heterogeneous type of disorder which can be caused due to environmental as well as genetical… 
Review
2013
Review
2013
Title: Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean… 
2010
2010
.............................................................................................................. ix 
2004
2004
Mutations in the myosin XVA gene (MYO15A) cause congenital non-syndromic deafness in humans and mice. Therefore, the MYO15A gene… 
2002
2002
The myosin superfamily includes conventional and unconventional myosin proteins. Among unconventional myosins, myosin XVA has…