Case Report: A combination of chimeric CYP11B2/CYP11B1 and a novel p.Val68Gly CYP11B1 variant causing 11β-Hydroxylase deficiency in a Chinese patient

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

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New Research: Case Report: A combination of chimeric CYP11B2/CYP11B1 and a novel p.Val68Gly CYP11B1 variant causing 11β-Hydroxylase deficiency in a Chinese patient: Introduction 11β-Hydroxylase deficiency (11β-OHD, OMIM#202010) is… https://t.co/Ts0IZ5QIWH

13 Nov 2023

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