deafness autosomal recessive type 16
deafness autosomal recessive type 16
An autosomal recessive form (OMIM:603720) of nonsyndromic sensorineural deafness,Molecular pathology Defects of STRC, which encodes a protein of the sensory hair cells in the inner ear involved with mechanoreception of sound waves, cause deafness autosomal recessive type 16.