DFNA5 Polyclonal Antibody, 50ul Variant Libraries Another member of this family
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DFNA5 Polyclonal Antibody, 50ul Variant Libraries Another member of this familyHearing impairment is a heterogeneous condition with over 40 loci described. Non syndromic hearing impairment protein 5 encoded by DFNA5 is expressed in fetal cochlea, however, its function is not known. Nonsyndromic hearing impairment is associated with a mutation in this gene. Three transcript variants encoding two different isoforms have been found for this gene.
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