An Atypical Case of Familial Glucocorticoid Deficiency without Pigmentation Caused by Coexistent Homozygous Mutations in MC2R (T152K) and MC1R (R160W)
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L. Metherell | A. Bereket | S. Turan | A. Clark | Z. Atay | T. Guran | B. Haliloglu | C. Hughes