Quantification of galactosylsphingosine in the twitcher mouse using electrospray ionization-tandem mass spectrometry

Globoid cell leukodystrophy (Krabbe disease) is an autosomal recessive inherited neurodegenerative disorder caused by the deficiency of the lysosomal enzyme β-galactosylceramidase. The pathogenesis of the disorder has been proposed to arise from the accumulation of the cytotoxic metabolite galactosy...

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Bibliographic Details
Main Authors: Phillip D. Whitfield, Peter C. Sharp, Rosanne Taylor, Peter Meikle
Format: Article
Language:English
Published: Elsevier 2001-12-01
Series:Journal of Lipid Research
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S002222752031539X