deafness autosomal dominant type 25

deafness autosomal dominant type 25

An autosomal dominant form (OMIM:605583) of nonsyndromic sensorineural deafness. 

Molecular pathology
Caused by defects of SLC17A8, which encodes a vesicle-bound glutamate transporter that transport glutamate into synaptic vesicles before its release into the synaptic cleft.
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