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DEAFNESS, AUTOSOMAL RECESSIVE 86
Known as:
DFNB86
National Institutes of Health
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Related topics
Related topics
1 relation
Autosomal recessive inheritance
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2017
Review
2017
Unresolved questions regarding human hereditary deafness.
A. Rehman
,
T. Friedman
,
A. Griffith
Oral diseases
2017
Corpus ID: 4479747
Human hearing loss is a common neurosensory disorder about which many basic research and clinically relevant questions are…
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Highly Cited
2014
Highly Cited
2014
Mutations in TBC1D24, a gene associated with epilepsy, also cause nonsyndromic deafness DFNB86.
A. Rehman
,
R. Santos-Cortez
,
+21 authors
T. Friedman
American journal of human genetics
2014
Corpus ID: 3066198
Review
2012
Review
2012
DFNB86, a novel autosomal recessive non‐syndromic deafness locus on chromosome 16p13.3
Rahima Ali
,
A. Rehman
,
+5 authors
S. Riazuddin
Clinical genetics
2012
Corpus ID: 43142864
To the Editor: We identified linkage of recessive pre-lingual deafness to a new locus, designated DFNB86. This linkage was…
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