Comment to 'Glucocorticoid resistance syndrome caused by a novel NR3C1 point mutation' by Al Argan et al

Endocr J. 2019 Jul 28;66(7):657. doi: 10.1507/endocrj.EJ19-0122. Epub 2019 Jun 13.

Authors

Salvatore Cannavò^{1

2}, Salvatore Benvenga^{3

4}, Erika Messina¹, Mariacarla Moleti^{1

3}, Francesco Ferraù^{1

2}

Affiliations

¹ Endocrine Unit, University Hospital of Messina, Italy.
² Department of Human Pathology, University of Messina, Italy.
³ Department of Clinical and Experimental Medicine, University of Messina, Italy.
⁴ Interdept. Program of Molecular & Clinical Endocrinology, University Hospital of Messina, Italy.

PMID: 31189748
DOI: 10.1507/endocrj.EJ19-0122

No abstract available

Publication types

Comment

MeSH terms

Glucocorticoids
Humans
Metabolism, Inborn Errors*
Point Mutation*
Receptors, Glucocorticoid

Substances

Glucocorticoids
NR3C1 protein, human
Receptors, Glucocorticoid