Familial Glucocorticoid Deficiency in Five Arab Kindreds with Homozygous Point Mutations of the ACTH Receptor (MC2R): Genotype and Phenotype Correlations

Publisher： Karger

E-ISSN： 1663-2826|76|3|165-171

ISSN： 1663-2818

Source： Hormone Research in Paediatrics, Vol.76, Iss.3, 2011-07, pp. : 165-171

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