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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English | 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
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Dorothea Götze
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Eckhard Korsch
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Manfred Rister
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Jens Commentz
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Carl-Joachim Partsch
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Joachim Grötzinger
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Michael Peter
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Wolfgang G Sippell
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8 March 2005
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