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Functional characterization of wild-type and mutated pendrin (SLC26A4), the anion transporter involved in Pendred syndrome.
J Mol Endocrinol. 2009 Sep;43(3):93-103. doi: 10.1677/JME-08-0175. Epub 2009 Jul 16.
J Mol Endocrinol. 2009.
PMID: 19608655
Review.
Molecular and functional characterization of human pendrin and its allelic variants.
Dossena S, Nofziger C, Tamma G, Bernardinelli E, Vanoni S, Nowak C, Grabmayer E, Kössler S, Stephan S, Patsch W, Paulmichl M.
Dossena S, et al. Among authors: grabmayer e.
Cell Physiol Biochem. 2011;28(3):451-66. doi: 10.1159/000335107. Epub 2011 Nov 18.
Cell Physiol Biochem. 2011.
PMID: 22116358
Free article.
Review.
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