Familial Glucocorticoid Deficiency Type 1 due to a Novel Compound Heterozygous MC2R Mutation | Citedby Results | Hormone Research in Paediatrics | Karger Publishers

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Familial Glucocorticoid Deficiency Type 1 due to a Novel Compound Heterozygous MC2R Mutation

Hormone Research (2008) 69 (6): 363–368.

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