Detection of Small CYP11B1 Deletions and One Founder Chimeric CYP11B2/CYP11B1 Gene in 11β-Hydroxylase Deficiency

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

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New Research: Detection of Small CYP11B1 Deletions and One Founder Chimeric CYP11B2/CYP11B1 Gene in 11β-Hydroxylase Deficiency: Objective 11β-Hydroxylase deficiency (11β-OHD) caused by mutations in the CYP11B1 gene is the second… https://t.co/74IjD00a41 #

24 May 2022

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