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Mechanisms and controversies in mutant Cul3-mediated familial hyperkalemic hypertension
Autosomal dominant mutations in cullin-3 (Cul3) cause the most severe form of familial hyperkalemic hypertension (FHHt). Cul3 mutations cause skipping of exon 9, which results in an internal deletion of 57 amino acids from the CUL3 protein (CUL3-∆9). The precise mechanism by which this altered form...
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| Udgivet i: | Am J Physiol Renal Physiol |
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| Main Authors: | , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
American Physiological Society
2018
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6031903/ https://ncbi.nlm.nih.gov/pubmed/29361671 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajprenal.00593.2017 |
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