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DEAFNESS, AUTOSOMAL RECESSIVE 86
Known as:
DFNB86
National Institutes of Health
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Topic mentions per year
2012-2017
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1
2012
2017
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1 relation
Autosomal recessive inheritance
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DEAFNESS, AUTOSOMAL RECESSIVE 86
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.
Atteeq Ur Rehman
,
Thomas B Friedman
,
A. Fanchamps. E. Fllickiger J. Grauwiler. R. W Griffith
Oral diseases
2017
Human hearing loss is a common neurosensory disorder about which many basic research and clinically relevant questions are…
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2014
2014
Mutations in TBC1D24, a gene associated with epilepsy, also cause nonsyndromic deafness DFNB86.
Atteeq Ur Rehman
,
Regie P. Lyn Santos-Cortez
,
+21 authors
Thomas B Friedman
American journal of human genetics
2014
Inherited deafness is clinically and genetically heterogeneous. We recently mapped DFNB86, a locus associated with nonsyndromic…
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2012
2012
DFNB86, a novel autosomal recessive non-syndromic deafness locus on chromosome 16p13.3.
Rana A. Ali
,
Atteeq Ur Rehman
,
+4 authors
Z M Ahmed
Clinical genetics
2012
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