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Deafness, Autosomal Recessive 3

Known as: DFNB3, NEUROSENSORY NONSYNDROMIC RECESSIVE DEAFNESS 3, NSRD3 
National Institutes of Health

Related topics

Related topics

2 relations
MYO15A, LYS1300TER

Broader (1)

Sensorineural Hearing Loss (disorder)

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Genetic Linkage Analysis of DFNB3, DFNB9 and DFNB21 Loci in GJB2 Negative Families with Autosomal Recessive Non-syndromic Hearing Loss
Background: Autosomal recessive non-syndromic hearing loss (ARNSHL) is the most common hereditary form of deafness, and exhibits… 
2014
2014
Study of the association of DFNB3 locus with autosomal recessive non-syndromic hearing loss in iranian deaf population using genetic linkage analysis
Background: Hearing loss is a common sensory disorder that typically illustrates genetic heterogeneity in human populations. The… 
2013
2013
Linkage study of DFNB3 responsible for hearing loss in human
BACKGROUND: Hearing disorders represent a significant health problem worldwide. Recessive inherited cases of the deafness are… 
2008
2008
Unexpected genetic heterogeneity in a large consanguineous Brazilian pedigree presenting deafness
Nonsyndromic autosomal recessive deafness accounts for 80% of hereditary deafness. To date, 52 loci responsible for autosomal… 
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