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DISORDERED ZONAL AND CELLULAR CYP11B2 ENZYME EXPRESSION IN FAMILIAL HYPERALDOSTERONISM TYPE 3
Three forms of familial primary aldosteronism have been recognized. Familial Hyperaldosteronism type 1 (FH1) or dexamethasone suppressible hyperaldosteronism, FH2, the most common form of as yet unknown cause(s), and FH3. FH3 is due to activating mutations of the potassium channel gene KCNJ5 that in...
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| Publicado no: | Mol Cell Endocrinol |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5123946/ https://ncbi.nlm.nih.gov/pubmed/27793677 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mce.2016.10.025 |
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