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 (Q45310697)

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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
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    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 (English)
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    Felix G Riepe
    Dorothea Götze
    Eckhard Korsch
    Manfred Rister
    Jens Commentz
    Carl-Joachim Partsch
    Joachim Grötzinger
    Michael Peter
    Wolfgang G Sippell
    8 March 2005
    3724-3730

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