A multicenter experience on the prevalence of ARMC5 mutations in patients with primary bilateral macronodular adrenal hyperplasia: from genetic characterization to clinical phenotype

N.M. Albiger, D. Regazzo, B. Rubin, A.M. Ferrara, S. Rizzati, E. Taschin, F. Ceccato, G. Arnaldi, F. Pecori Giraldi, A. Stigliano, L. Cerquetti, F. Grimaldi, E. De Menis, M. Boscaro, M. Iacobone, G. Occhi, C. Scaroni

Research output: Contribution to journalArticle

Original languageItalian
Pages (from-to)959-968
Number of pages10
JournalEndocrine
Volume55
Issue number3
DOIs
Publication statusPublished - 2017

Cite this

Albiger, N. M., Regazzo, D., Rubin, B., Ferrara, A. M., Rizzati, S., Taschin, E., Ceccato, F., Arnaldi, G., Pecori Giraldi, F., Stigliano, A., Cerquetti, L., Grimaldi, F., De Menis, E., Boscaro, M., Iacobone, M., Occhi, G., & Scaroni, C. (2017). A multicenter experience on the prevalence of ARMC5 mutations in patients with primary bilateral macronodular adrenal hyperplasia: from genetic characterization to clinical phenotype. Endocrine, 55(3), 959-968. https://doi.org/10.1007/s12020-016-0956-z