The underlying cause of the simple virilizing phenotype in patients with 21-hydroxylase deficiency harboring P31L variant

Overview of attention for article published in Frontiers in endocrinology, February 2023

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New Research: The underlying cause of the simple virilizing phenotype in patients with 21-hydroxylase deficiency harboring P31L variant: Objective To analyze the relationship between genotype and phenotype in 21-Hydroxylase… https://t.co/m7lnmD8DeF #Endoc

14 Feb 2023

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