Presenting Features, Clinical Characteristics and Follow Up of Familial Isolated Glucocorticoid Deficiency (FGD) Due to Mutations in MC2R and MRAP Genes | AVESİS

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Presenting Features, Clinical Characteristics and Follow Up of Familial Isolated Glucocorticoid Deficiency (FGD) Due to Mutations in MC2R and MRAP Genes

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Ozbek M. N., Karasin N. D., DEMİRBİLEK H., Demiral M., Baran R. T., GÜRAN T.

HORMONE RESEARCH IN PAEDIATRICS, vol.90, pp.161-162, 2018 (SCI-Expanded)

Publication Type: Article / Abstract
Volume: 90
Publication Date: 2018
Journal Name: HORMONE RESEARCH IN PAEDIATRICS
Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
Page Numbers: pp.161-162
Hacettepe University Affiliated: Yes