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Overview
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Calculated MW: 66kDa
Observed MW: 66kDaPlease contact us at for specific academic pricing.
Background
Hearing impairment is a heterogeneous condition with over 40 loci described. The protein encoded by this gene 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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- Properties
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Overview