Failure of Fluid Absorption in the Endolymphatic Sac Initiates Cochlear Enlargement that Leads to Deafness in Mice Lacking Pendrin Expression

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Pendrin

Cited by user Trisbret on 05 Apr 2017

Pendrin, is an anion exchange protein that in humans is encoded by the SLC26A4 gene (solute carrier family 26, member 4).