Functional and structural consequences of a novel point mutation in the CYP21A2 gene causing congenital adrenal hyperplasia: Potential relevance of helix C for p450 oxidoreductase-21-hydroxylase interaction
FG Riepe, O Hiort, J Groetzinger, WG Sippell, Nils Krone, PM Holterhus
Research output: Contribution to journal › Article
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