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MYO1A gene

Known as: MYO1A, MYOSIN IA 
National Institutes of Health

Related topics

Related topics

2 relations
MYO18B geneMYO1A protein, human

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
A genotypic ascertainment approach to refute the association of MYO1A variants with non-syndromic deafness
Variants in the unconventional myosin gene, MYO1A, have been reported to cause non-syndromic sensorineural hearing loss with a… 
2014
2014
Targeted and Genomewide NGS Data Disqualify Mutations in MYO1A, the “DFNA48 Gene”, as a Cause of Deafness
MYO1A is considered the gene underlying autosomal dominant nonsyndromic hearing loss DFNA48, based on six missense variants, one… 
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