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DEAFNESS, AUTOSOMAL RECESSIVE 86
National Institutes of Health
Autosomal recessive inheritance
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Unresolved questions regarding human hereditary deafness.
Corpus ID: 4479747
Human hearing loss is a common neurosensory disorder about which many basic research and clinically relevant questions are…
Mutations in TBC1D24, a gene associated with epilepsy, also cause nonsyndromic deafness DFNB86.
R. L. Santos-Cortez
American journal of human genetics
Corpus ID: 3066198
Inherited deafness is clinically and genetically heterogeneous. We recently mapped DFNB86, a locus associated with nonsyndromic…
DFNB86, a novel autosomal recessive non‐syndromic deafness locus on chromosome 16p13.3
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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