Genetic basis of hearing loss associated with enlarged vestibular aqueducts in Koreans
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2004.00386.x/fullpdf
Reference25 articles.
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3. Pendrin, the protein encoded by the Pendred syndrome gene (PDS), is an apical porter of iodide in the thyroid and is regulated by thyroglobulin in FRTL-5 cells;Royaux;Endocrinology,2000
4. Pendrin, encoded by the Pendred syndrome gene, resides in the apical region of renal intercalated cells and mediates bicarbonate secretion;Royaux;Proc Natl Acad Sci USA,2001
5. Pendrin: an apical Cl-/OH-/HCO3-exchanger in the kidney cortex;Soleimani;Am J Physiol Renal Physiol,2001
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