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A novel germline ARMC5 mutation in a patient with bilateral macronodular adrenal hyperplasia: a case report
BACKGROUND: Bilateral macronodular adrenal hyperplasia (BMAH) is a rare cause of Cushing’s syndrome (CS). BMAH is predominantly believed to be caused by two mutations, a germline and somatic one, respectively, as described in the two-hit hypothesis. In many familial cases of BMAH, mutations in armad...
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| Publicat a: | BMC Med Genet |
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| Autors principals: | , , , , , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5870939/ https://ncbi.nlm.nih.gov/pubmed/29587644 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-018-0564-2 |
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