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CYP450 21A2-Mutation

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Lexikon der Medizinischen Laboratoriumsdiagnostik

Part of the book series: Springer Reference Medizin ((SRM))

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CYP450 21A2-Mutation

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Literatur

  • El-Maouche D, Arlt W, Merke DP (2017) Congenital adrenal hyperplasia. Lancet 11;390(10108):2194–2210

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  • Pallan PS, Wang C, Lei L, Yoshimoto FK, Auchus RJ, Waterman MR, Guengerich FP, Egli M (2015) Human Cytochrome P450 21A2, the Major Steroid 21-Hydroxylase: structure of the enzyme progesterone substrate complex and rate-limiting C–H bond cleavage. J Biol Chem 290(21):13128–13143

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Author information

Authors and Affiliations

  1. Medizinische Klinik und Poliklinik IV, Klinikum der Universität München, München, Deutschland

    M. Bidlingmaier

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  1. M. Bidlingmaier
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Correspondence to M. Bidlingmaier .

Editor information

Editors and Affiliations

  1. Labor Dr. Wisplinghoff, Berlin, Germany

    Axel M. Gressner

  2. Bioscientia Inst. Medizinische Diagnostik GmbH, Ingelheim, Germany

    Torsten Arndt

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© 2018 Springer-Verlag GmbH Deutschland, ein Teil von Springer Nature

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Bidlingmaier, M. (2018). CYP450 21A2-Mutation. In: Gressner, A., Arndt, T. (eds) Lexikon der Medizinischen Laboratoriumsdiagnostik. Springer Reference Medizin. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-49054-9_810-1

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  • DOI: https://doi.org/10.1007/978-3-662-49054-9_810-1

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  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-662-49054-9

  • Online ISBN: 978-3-662-49054-9

  • eBook Packages: Springer Referenz Medizin

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