Revisiting the diagnosis: HNF1β mutation masquerading as Gitelman syndrome

CEN Case Reports 2026 Open access

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Authors: Tahsin Özpolat, Muzammel Hada, Ali Rıza Köksal, Golnaz Vahdani
DOI: 10.1007/s13730-025-01083-1
Cited by: 0
References: 1

Fields of Study & Subjects

Ion Transport and Channel Regulation Genomics and Rare Diseases Renal Diseases and Glomerulopathies

Publication details

Journal / source
CEN Case Reports
Volume
15
Issue
2
Pages
49–49
Publication date
9 February 2026
Language
EN