deafness autosomal recessive type 79
deafness autosomal recessive type 79
A severe to profound autosomal recessive form (OMIM:613307) of prelingual nonsyndromic sensorineural hearing loss.
Molecular pathology
Defects of TPRN, which encodes a sensory epithelial protein, cause deafness autosomal recessive type 79.Segen's Medical Dictionary. © 2012 Farlex, Inc. All rights reserved.
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