Three novel point mutations of the CYP21 gene detected in classical forms of congenital adrenal hyperplasia due to 21-hydroxylase deficiency

N Krone, F G Riepe, C-J Partsch, W Vorhoff, J Brämswig, W G Sippell

    Research output: Contribution to journal › Article › peer-review

    10 Citations (Scopus)

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    Medicine & Life Sciences