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Insights into the diverse mechanisms and effects of variant CUL3-induced familial hyperkalemic hypertension
Familial hyperkalemic hypertension (FHHt), also known as Pseudohypoaldosteronism type II (PHAII) or Gordon syndrome is a rare Mendelian disease classically characterized by hyperkalemia, hyperchloremic metabolic acidosis, and high systolic blood pressure. The most severe form of the disease is cause...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2023
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10577937/ https://www.ncbi.nlm.nih.gov/pubmed/37845702 http://dx.doi.org/10.1186/s12964-023-01269-z |