WNK kinases regulate thiazide-sensitive Na-Cl cotransport
Pseudohypoaldosteronism type II (PHAII) is an autosomal dominant disorder of hyperkalemia and hypertension. Mutations in two members of the WNK kinase family, WNK1 and WNK4, cause the disease. WNK1 mutations are believed to increase WNK1 expression; the effect of WNK4 mutations remains unknown. The...
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| Pubblicato in: | J Clin Invest |
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| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
American Society for Clinical Investigation
2003
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC152590/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/12671053/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI17443 |
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