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Hong Sang Choi, Sang Heon Suh, Chang Seong Kim, Seong Kwon Ma, Soo Wan Kim, Eun Hui Bae
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The variety of genetic defects explains the phenotypic heterogeneity of familial hyperkalemic hypertension
10.1016/j.ekir.2021.07.025 · 2021
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities
10.1038/nature10814 · 2012
The CUL3-KLHL3 E3 ligase complex mutated in Gordon's hypertension syndrome interacts with and ubiquitylates WNK isoforms: disease-causing mutations in KLHL3 and WNK4 disrupt interaction
10.1042/bj20121903 · 2013
The CUL3-KLHL3 E3 ligase complex mutated in Gordon's hypertension syndrome interacts with and ubiquitylates WNK isoforms: disease-causing mutations in KLHL3 and WNK4 disrupt interaction
10.1042/bj20121903 · doi-reference
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities
10.1038/nature10814 · doi-reference
The variety of genetic defects explains the phenotypic heterogeneity of familial hyperkalemic hypertension
10.1016/j.ekir.2021.07.025 · doi-reference
Confidence 100%
pubmed
Confidence 98%
europepmc
Confidence 96%
openalex
Confidence 95%
datacite
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