Clinical characteristics and molecular etiology of partial 17α-hydroxylase deficiency diagnosed in 46,XX patients

Overview of attention for article published in Frontiers in endocrinology, December 2022

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New Research: Clinical characteristics and molecular etiology of partial 17α-hydroxylase deficiency diagnosed in 46,XX patients: Introduction Complete 17α-hydroxylase deficiency (17OHD) is relatively common, with typical juvenile… https://t.co/hXRgkAzUY4

16 Dec 2022

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