A Novel Homozygous KLHL3 Mutation as a Cause of Autosomal Recessive Pseudohypoaldosteronism Type II Diagnosed Late in Life

Etges, Annika Hellmig, Nicole Walenda, Gudrun Haddad, Bassam G. Machtens, Jan-Philipp Morosan, Thomas Rump, Lars Christian Scholl, Ute I.

528500-3 080012 929330

Nephron

Karger

Basel

2235-3186

10.1159/000521626

English 418-428 4 146 0, ; PUB:(DE-HGF)16, ;

WOS:000750626400001

Journal Article

2022

RWTH-CONV-251131

2022 pmid:35093948

https://publications.rwth-aachen.de/record/953616 https://doi.org/10.1159/000521626 <Go to ISI>://WOS:000750626400001