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Neuroglycobiology$
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Minoru Fukuda, Urs Rutishauser, and Ronald L. Schnaar

Print publication date: 2005

Print ISBN-13: 9780198525387

Published to Oxford Scholarship Online: September 2009

DOI: 10.1093/acprof:oso/9780198525387.001.0001

Lysosomal glycosphingolipid storage diseases

Chapter:
(p. 199 ) Chapter 8 Lysosomal glycosphingolipid storage diseases
Source:
Neuroglycobiology
Author(s):

Thomas Kolter

Konrad Sandhoff

Publisher:
Oxford University Press
DOI:10.1093/acprof:oso/9780198525387.003.0008

This chapter focuses on the catabolism of glycolipids and diseases caused by anomalies in this process. Topics covered include lysosomal storage diseases, glycosphingolipids, mechanism of lysosomal glycosphingolipid degradation, defects of glycosphingolipid catabolism, and general aspects of sphingolipidoses.

Keywords:   catabolism, glycolipids, lysosomal storage diseases, glycosphingolipids, sphingolipidoses

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