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Glutaminsäure-Decarboxylase in Hautfibroblasten von Huntington-Patienten und Kontrollpersonen

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Verhandlungen der Deutschen Gesellschaft für Neurologie

Part of the book series: Verhandlungen der Deutschen Gesellschaft für Neurologie ((VDGNEUROLOGIE,volume 5))

Zusammenfassung

Inzwischen ist bekannt, daß das pathologische Gen für Huntington-Patienten auf dem Chromosom 4 liegt. Die genetische Beratung gestaltet sich dennoch sehr schwierig, da umfangreiche DNA-Untersuchungen durchgeführt werden müssen, und z.Z. auch noch mehrere Familiengenerationen notwendig sind, bevor ein Ergebnis mitgeteilt werden kann.

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Literatur

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Authors
  1. H. Przuntek
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  2. M. Gerlach
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  3. H. Lange
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  4. W. Kuhn
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  5. C. Endres
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Editor information

Editors and Affiliations

  1. Zentrum der Neurologie und Neurochirurgie, Abteilung für Neurologie, Klinikum der Universität Frankfurt, Schleusenweg 2-16, D-6000, Frankfurt/Main 71, Germany

    Peter-Alexander Fischer , Horst Baas  & Wolfgang Enzensberger ,  & 

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© 1989 Springer-Verlag Berlin Heidelberg

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Przuntek, H., Gerlach, M., Lange, H., Kuhn, W., Endres, C. (1989). Glutaminsäure-Decarboxylase in Hautfibroblasten von Huntington-Patienten und Kontrollpersonen. In: Fischer, PA., Baas, H., Enzensberger, W. (eds) Verhandlungen der Deutschen Gesellschaft für Neurologie. Verhandlungen der Deutschen Gesellschaft für Neurologie, vol 5. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-83771-5_184

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  • DOI: https://doi.org/10.1007/978-3-642-83771-5_184

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-540-51091-8

  • Online ISBN: 978-3-642-83771-5

  • eBook Packages: Springer Book Archive

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