Open AccessLIDDLE SYNDROME – DETECTION OF NOVEL MUTATION IN A FAMILY WITH HYPERTENSION
Author(s) -
Jan Filipovský,
Štěpán Mareš,
Martin Pešta,
Jaroslav Hrabák
Publication year - 2021
Publication title -
journal of hypertension
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.249
H-Index - 172
eISSN - 1473-5598
pISSN - 0263-6352
DOI - 10.1097/01.hjh.0000747488.65621.9f
Subject(s) - hypokalemia , epithelial sodium channel , medicine , aldosterone , endocrinology , distal convoluted tubule , reabsorption , renal sodium reabsorption , plasma renin activity , mutation , pseudohypoaldosteronism , homeostasis , bartter syndrome , renin–angiotensin system , kidney , blood pressure , genetics , gene , sodium , biology , chemistry , organic chemistry