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DEAFNESS, AUTOSOMAL RECESSIVE 49

Known as: DFNB49 
An autosomal recessive disorder caused by mutations in the MARVELD2 gene, encoding MARVEL domain-containing protein 2. The condition is characterized… 
National Institutes of Health

Related topics

Related topics

4 relations
Autosomal recessive inheritanceEar structureHead and neck structure

Broader (1)

Sensorineural Hearing Loss (disorder)

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Segregation of DFNB 49 with congenital sensorineural bilateral profound hearing loss
Deafness is a complete or partial loss of hearing. In Pakistan, the prevalence of this order is high as compared to the other… 
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