Presenting Features, Clinical Characteristics andFollow Up of Familial Isolated GlucocorticoidDeficiency (FGD) Due to Mutations in MC2R andMRAP Genes


ozbek m. n. , doğan karaşin n., DEMİRBİLEK H., demiral m., BARAN R. T. , GÜRAN T.

57th Annual Meeting of ESPE (European Society for Pediatric Endocrinology, 27 - 29 Eylül 2018