Pendrin Function and Regulation in Xenopus Oocytes

SLC26A4/PDS mutations cause Pendred Syndrome and non-syndromic deafness. but some aspects of function and regulation of the SLC26A4 polypeptide gene product, pendrin, remain controversial or incompletely understood. We have therefore extended the functional analysis of wildtype and mutant pendrin in...

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Main Authors: Reimold, Fabian R., Heneghan, John F., Stewart, Andrew K., Zelikovic, Israel, Vandorpe, David H., Shmukler, Boris E., Alper, Seth L.
Formáid: Artigo
Teanga:Inglês
Foilsithe: S. Karger AG 2011
Ábhair:
Original Paper
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3709188/
https://ncbi.nlm.nih.gov/pubmed/22116357
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000335106
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