Associated Papers
The variety of genetic defects explains the phenotypic heterogeneity of Familial Hyperkalemic Hypertension.
Hureaux M et al.
Kidney International Reports, 2021
34622103 (PubMed )
Supplement: mmc1.pdf
[Causative genetic variants of pseudohypoaldosteronism type II and essential hypertension].
Mori T et al.
Nihon Jinzo Gakkai Shi, 2015
Development of enzyme-linked immunosorbent assays for urinary thiazide-sensitive Na-Cl cotransporter measurement.
Isobe K et al.
American Journal of Physiology. Renal Physiology, 2013
[Pseudohypoaldosteronism type II].
Endoh A
Nihon Rinsho. Japanese Journal of Clinical Medicine, 2006
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