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Two mutations in the thiazide-sensitive NaCl co-transporter gene in a Romanian Gitelman syndrome patient: case report

Cristina Gug1, Adelina Mihaescu2, Ioana Mozos3,4

  • 1Department of Microscopic Morphology.

Therapeutics and Clinical Risk Management
|February 7, 2018
PubMed
Abstract

Keywords:
Gitelman syndromeSLC12A3 geneconsanguinityhirsutismhypokalemiahypomagnesemia

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