From The Cover: Galactocerebrosidase-deficient oligodendrocytes maintain stable central myelin by exogenous replacement of the missing enzyme in mice
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference38 articles.
1. Globoid Cell Leucodystrophy (Krabbe's Disease): Deficiency of Galactocerebroside -Galactosidase
2. HEREDITARY LEUCODYSTROPHY IN THE MOUSE: THE NEW MUTANT TWITCHER
3. The twitcher mouse: an enzymatically authentic model of human globoid cell leukodystrophy (Krabbe disease)
4. Molecular Cloning and Expression of cDNA for Murine Galactocerebrosidase and Mutation Analysis of the Twitcher Mouse, a Model of Krabbe's Disease
5. The Twitcher Mouse: A Model for Krabbe Disease and for Experimental Therapies
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