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References from The Case | Persistent hyperkalemia in a normotensive woman. Local targets link to admitted publications; unresolved targets remain external evidence.
The variety of genetic defects explains the phenotypic heterogeneity of familial hyperkalemic hypertension
10.1016/j.ekir.2021.07.025 · 2021 · External reference
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities
10.1038/nature10814 · 2012 · External reference
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 · External reference
The variety of genetic defects explains the phenotypic heterogeneity of familial hyperkalemic hypertension
10.1016/j.ekir.2021.07.025 · ExternalCitation · doi-reference
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities
10.1038/nature10814 · ExternalCitation · doi-reference
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 · ExternalCitation · doi-reference
