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Overview
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Calculated MW: 53kDa/165kDa
Observed MW: 165kDaPlease contact us at for specific academic pricing.
Background
This gene encodes a transmembrane connexin protein that is a component of gap junctions. Mutations in this gene have been associated with erythrokeratodermia variabilis, progressive symmetric erythrokeratoderma and hearing impairment.
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