The functional study of novel KLHL3 missense mutations associated with pseudohypoaldosteronism type II.
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DOI: 10.1007/s12020-025-04456-9
Abstract: Pseudohypoaldosteronism type II (PHA II) is an inherited tubulopathy, clinically defined by three hallmark features, including secondary hypertension, hyperchloremic metabolic acidosis, and persistent hyperkalemia occurring despite maintained glomerular filtration function. Herein, we aim to investigate… read more here.
Keywords: klhl3; pseudohypoaldosteronism type; study; functional study ... See more keywords