Open AccessMutations of the PDS Gene, Encoding Pendrin, Are Associated with Protein Mislocalization and Loss of Iodide Efflux: Implications for Thyroid Dysfunction in Pendred Syndrome
Author(s) -
Julie P. Taylor
Publication year - 2002
Publication title -
the journal of clinical endocrinology and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.206
H-Index - 353
eISSN - 1945-7197
pISSN - 0021-972X
DOI - 10.1210/jc.87.4.1778
Subject(s) - pendrin , thyroid , endocrinology , medicine , mutant , iodide , biology , chemistry , gene , genetics , transporter , organic chemistry
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