Turkish Journal of Medical Sciences
Author ORCID Identifier
SAİDE ELİFGÖKHAN GÜLLÜLÜ BOZÖNGEN: 0000-0001-6048-1879
HANDE AYPEK: 0000-0002-3767-475X
GÜLŞAH ÇEÇENER: 0000-0002-3820-424X
ALPARSLAN ERSOY: 0000-0002-0710-0923
ABDULMECİT YILDIZ: 0000-0001-5941-9103
DOI
10.55730/1300-0144.6410
Keywords
Autosomal Dominant Polycystic Kidney Disease (ADPKD), dapagliflozin, intrafamilial variability, PKD1, Sodium-glucose cotransporter-2 (SGLT2) inhibitors
First Page
1632
Last Page
1635
Publisher
The Scientific and Technological Research Council of Türkiye (TÜBİTAK)
Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 International License.
Recommended Citation
GÜLLÜLÜ BOZ, S, AYPEK, H, ÖNGEN, G, ÇEÇENER, G, ERSOY, A, & YILDIZ, A (2026). Intrafamilial variability in autosomal dominant polycystic kidney disease due to a shared PKD1 mutation: a potential signal of sodium-glucose cotransporter-2 (SGLT2) inhibitor benefit . Turkish Journal of Medical Sciences 56 (5): 1632-1635. https://doi.org/10.55730/1300-0144.6410
