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Dive into the research topics of 'A mutation in CYP11B1 (Arg-448 → His) associated with steroid 11β-hydroxylase deficiency in jews of Moroccan origin'. Together they form a unique fingerprint.- Sort by
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Perrin C. White, Jakob Dupont, Maria I. New, Esther Leiberman, Zeev Hochberg, Ariel Rösler
Research output: Contribution to journal › Article › peer-review