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DEAFNESS, AUTOSOMAL RECESSIVE 13

Known as: DFNB13 
National Institutes of Health

Related topics

Related topics

3 relations
Autosomal recessive inheritanceDFNB13 gene

Broader (1)

Sensorineural Hearing Loss (disorder)

Papers overview

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1998
1998
A sensorineural progressive autosomal recessive form of isolated deafness, DFNB13, maps to chromosome 7q34-q36
Deafness is the most frequent sensorineural defect in children. The vast majority of the prelingual forms of isolated deafness… 
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