Association of p.His38Leu, a Rare CYP21A2 Mutation, with the Classical Simple Virilizing Phenotype of 21-Hydroxylase Deficiency in a 6-Year-Old Boy

Publisher： Karger

E-ISSN： 1663-2826|76|3|214-217

ISSN： 1663-2818

Source： Hormone Research in Paediatrics, Vol.76, Iss.3, 2011-09, pp. : 214-217

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