deafness autosomal recessive type 24

deafness autosomal recessive type 24

An autosomal recessive form (OMIM:611022) of nonsyndromic sensorineural deafness.

Molecular pathology
Caused by defects of RDX, which encodes radixin, a cytoskeletal protein that may be important in linking the barbed end of actin filaments to the plasma membrane.
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