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Molecular mechanisms of ARMC5 mutations in adrenal pathophysiology
Since the initial discovery of mutations in the Armadillo-containing repeat protein 5 gene (ARMC5) in primary bilateral macronodular adrenocortical hyperplasia (PBMAH), efforts have been made to better understand the molecular mechanisms involving ARMC5 in the development of this rare form of Cushin...
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| Veröffentlicht in: | Curr Opin Endocr Metab Res |
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| Hauptverfasser: | , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2019
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7448540/ https://ncbi.nlm.nih.gov/pubmed/32864505 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.coemr.2019.07.010 |
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