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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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Detaylı Bibliyografya
Asıl Yazarlar: Phillip D. Whitfield, Peter C. Sharp, Rosanne Taylor, Peter Meikle
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Elsevier 2001-12-01
Seri Bilgileri:Journal of Lipid Research
Konular:
Online Erişim:http://www.sciencedirect.com/science/article/pii/S002222752031539X
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