Enzyme alterations and lipid storage in three variants of Tay-Sachs disease.

Journal of neurochemistry ·Vol. 18 ·No. 12 ·1971-12-00 ·Pages 2469-89

Sandhoff K, Harzer K, Wässle W, Jatzkewitz H

Abstract

暂无摘要

MeSH Terms

Brain/enzymology Brain Chemistry Ceramides/analysis Child, Preschool Chromatography, Ion Exchange Chromatography, Thin Layer Galactosamine Gangliosides/analysis Glycolipids/analysis Glycoside Hydrolases/metabolism Hexosaminidases/metabolism Hexoses Hot Temperature Humans Hydrogen-Ion Concentration Infant Isoelectric Focusing Kidney/analysis,enzymology Lipid Metabolism Lipidoses/enzymology,metabolism Liver/analysis,enzymology

Chemicals

Ceramides Gangliosides Glycolipids Hexoses Galactosamine Glycoside Hydrolases Hexosaminidases

Authors & Affiliations

4 authors, click to expand affiliations / ORCID

Sandhoff K

Harzer K

Wässle W

Jatzkewitz H

Article Info

Journal

Journal of neurochemistry

Abbr.

J Neurochem

ISSN

0022-3042

DOI

10.1111/j.1471-4159.1971.tb00204.x

Published

1971-12-00

Pages

2469-89

Language

English

Region

England

NLM ID

2985190R

Subset

External Links

PubMed source DOI: 10.1111/j.1471-4159.1971.tb00204.x View journal details

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Enzyme alterations and lipid storage in three variants of Tay-Sachs disease.

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