Alencar GA et al. ARMC5 mutations are a frequent cause of primary macronodular adrenal hyperplasia. J Clin Endocrinol Metab. 2014;99(8):E1501-9. PMID: 24708098.
Assié G et al. ARMC5 mutations in macronodular adrenal hyperplasia with Cushing’s Syndrome. N Engl J Med. 2013;369(22):2105-14. PMID: 24283224.
Berthon A et al. Age-dependent effects of ARMC5 haploinsufficiency on adrenocortical function. Hum Mol Genet. 2017;26(18):3495-3507. PMID: 28911199.
Faucz FR et al. Macronodular adrenal hyperplasia due to mutations in armadillo repeat containing 5 (ARMC5) gene: a clinical and genetic investigation. J Clin Endocrinol Metab. 2014;99:E1113-9. PMID: 24601692.
Stratakis CA et al. Clinical and genetic analysis of primary bilateral adrenal diseases (micro-and macronodular disease) leading to Cushing syndrome. Horm Metab Res. 1998;30:456-463. PMID: 9694579.
Correa et al. The ARMC5 gene shows extensive genetic variance in primary macronodular adrenocortical hyperplasia. Eur J Endocrinol. 2015;173(4):435-40. PMID: 26162405.