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Deafness, Autosomal Dominant 48

Known as: DFNA48 
National Institutes of Health

Related topics

Related topics

2 relations
Autosomal dominant inheritance

Broader (1)

Sensorineural Hearing Loss (disorder)

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
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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