Molecular Basis, Diagnostic Challenges and Therapeutic Approaches of Bartter and Gitelman Syndromes: A Primer for Clinicians
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DOI: 10.3390/ijms222111414
Abstract: Gitelman and Bartter syndromes are rare inherited diseases that belong to the category of renal tubulopathies. The genes associated with these pathologies encode electrolyte transport proteins located in the nephron, particularly in the Distal Convoluted… read more here.
Keywords: basis diagnostic; molecular basis; diagnostic challenges; therapeutic approaches ... See more keywords