Oligosaccharides accumulating in the liver from a patient with GM2-gangliosidosis variant 0 (Sandhoff-Jatzkewitz disease)
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference14 articles.
1. Deficient hexosaminidase activity in an exceptional case of Tay-Sachs disease with additional storage of kidney globoside in visceral organs
2. GM2-gangliosidosis with total hexosaminidase deficiency
3. Description d'une oligosaccharidosurie accompagnant une gangliosidose gm 2 á déficit total en 1v-acétyl-hexosaminidases
4. The Structures of Oligosaccharides Accumulating in the Liver of G1-Gangliosidosis, Type I
5. Analysis of neutral sugars by gas-liquid chromatography of alditol acetates: Application to thyrotropic hormone and other glycoproteins
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1. Natural history study of glycan accumulation in large animal models of GM2 gangliosidoses;PLOS ONE;2020-12-01
2. Catabolism of N-glycoproteins in mammalian cells: Molecular mechanisms and genetic disorders related to the processes;Molecular Aspects of Medicine;2016-10
3. Degradation of keratan sulfate by ß-N-acetylhexosaminidases in GM2-gangliosidosis;Clinical Genetics;2008-04-23
4. Cultured fucosidosis fibroblasts: A simple technique demonstrating storage of tritiated-fucose labeled material;Clinical Genetics;2008-04-23
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