Congenital adrenal hyperplasia due to 11-hydroxylase deficiency: functional characterization of two novel point mutations and a three-base pair deletion in the CYP11B1 gene
Nils Krone, Felix G Riepe, Dorothea Götze, Eckhard Korsch, Manfred Rister, Jens Commentz, Carl-Joachim Partsch, Joachim Grötzinger, Michael Peter, Wolfgang G Sippell
Research output: Contribution to journal › Article › peer-review
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