Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations (vol 22, pg 610, 2020)
EUROPEAN JOURNAL OF HUMAN GENETICS(2020)
摘要
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
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Biomedicine,general,Human Genetics,Bioinformatics,Gene Expression,Cytogenetics
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