An Asian case of combined 17α-hydroxylase/17,20-lyase deficiency due to homozygous p.R96Q mutation: A case report and review of the literature

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

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https://t.co/k14ODzJh36 https://t.co/5WSC4OdqKo

09 Nov 2022

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New Research: An Asian case of combined 17α-hydroxylase/17,20-lyase deficiency due to homozygous p.R96Q mutation: A case report and review of the literature: Background Combined 17α-hydroxylase/17,20-lyase deficiency (17-OHD) is a… https://t.co/IUDyGceZnj

19 Oct 2022

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