Two mutations in the thiazide-sensitive NaCl co-transporter gene in a Romanian Gitelman syndrome patient: case report
Cristina Gug,1 Adelina Mihaescu,2 Ioana Mozos3,4 1Department of Microscopic Morphology, 22nd Department of Internal Medicine, 3Department of Functional Sciences, 4Center for Translational Research and Systems Medicine, “Victor Babes” University of Medicine and Pharmacy, Timisoar...
Main Authors: | Gug C, Mihaescu A, Mozos I |
---|---|
Format: | Article |
Language: | English |
Published: |
Dove Medical Press
2018-01-01
|
Series: | Therapeutics and Clinical Risk Management |
Subjects: | |
Online Access: | https://www.dovepress.com/two-mutations-in-the-thiazide-sensitive-nacl-co-transporter-gene-in-a--peer-reviewed-article-TCRM |
Similar Items
-
Two Brothers from Macedonia with Gitelman Syndrome
by: Janchevska A, et al.
Published: (2023-07-01) -
Three uncommon mutations of the SLC12A3 gene in gitelman syndrome: case reports and review of the literature
by: Melis Akpinar Gozetici, et al.
Published: (2022-04-01) -
Gitelman syndrome DD thiazide diuretics abuse
by: Keller Karsten, et al.
Published: (2014-06-01) -
Molecular complexity analysis of the diagnosis of Gitelman syndrome in China
by: Song Wei, et al.
Published: (2023-06-01) -
GITELMAN SYNDROME AS A RARE CAUSE OF HYPOKALEMIA - CASE REPORT
by: Zorica Dimitrijević, et al.
Published: (2014-09-01)