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Hearing impairment is a heterogeneous condition with over 40 loci described. DFNA5 encodes a protein expressed in fetal cochlea of unknown function. Nonsyndromic hearing impairment is associated with a mutation in DFNA5.
Gene Name: | deafness, autosomal dominant 5 |
Synonyms: | DFNA5, ICERE-1, Deafness, autosomal dominant 5, ICERE1 |
Target Sequences: | NM_004403 NP_004394.1 O60443 |
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