alexa Deletion of the C4-CYP21 repeat module leading to the formation of a chimeric CYP21P CYP21 gene in a 9.3-kb fragment as a cause of steroid 21-hydroxylase deficiency.
Genetics & Molecular Biology

Genetics & Molecular Biology

Human Genetics & Embryology

Author(s): Lee HH, Chang SF, Lee YJ, Raskin S, Lin SJ,

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This article was published in Clin Chem and referenced in Human Genetics & Embryology

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