The use of globotriaosylsphingosine to detect and monitor Fabry disease

Fabry disease (FD) is an X-linked lysosomal storage disorder caused by a deficiency of the α-galactosidase-A (α-gal-A) enzyme. The lack of enzymatic activity results in the accumulation of glycosphingolipids (GSLs) in the lysosomes of various tissues and organs. Globotriaosylceramide (Gb3) and Globo...

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Bibliographic Details
Main Author: Alharbi, Fahad Jazza
Published: University of Birmingham 2016
Subjects:
Online Access:https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.694738

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