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Accessibility Gitelman syndrome is a rare autosomal recessive salt-losing tubulopathy characterized by hypokalemia, hypomagnesemia, hypocalciuria, and secondary hyperaldosteronism. OnlineFirst chapter in a series (without a volume designation but with a DOI). Book chapter, or an article within a book. Online Publication Date: 27 Jan 2021, Familial GATA6 mutation causing variably expressed diabetes mellitus and cardiac and renal abnormalities, Authors: Yang Timothy Du, Lynette Moore, Nicola K Poplawski, and Sunita M C De Sousa
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Case Presentation. Endocrine Connections is a society-owned open access journal offering authors the highest possible visibility for their work and stimulating cross-discipline collaboration. 2013;11:63. To our best knowledge, this is the first report in English of a patient with ARVC showing refractory arrhythmia induced by thyroid storm due to Graves disease. Case Reports in Endocrinology maintains an Editorial Board of practicing researchers from around the world, to ensure manuscripts are handled by editors who are experts in the field of study. Authors should obtain permission to acknowledge from all those mentioned in the Acknowledgements section. Not applicable. All data generated or analysed during this study are included in this published article [and its supplementary information files]. See our editorial policies for more information on consent for publication. Online Publication Date: 03 May 2019. 1999. http://www.rsc.org/dose/title of subordinate document. 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