Deficient hexozaminidase activity in an exceptional case of Tay-Sachs disease with additional storage of kidney globoside in visceral organs.

Life sciences ·Vol. 7 ·No. 6 ·1968-03-15 ·Pages 283-8

Sandhoff K, Andreae U, Jatzkewitz H

Abstract

暂无摘要

MeSH Terms

Aminohydrolases/metabolism Brain Chemistry Child, Preschool Chromatography, Thin Layer Glycolipids/analysis Hexosamines/metabolism Humans Kidney/metabolism Lipidoses/complications,enzymology Male

Chemicals

Glycolipids Hexosamines Aminohydrolases

Authors & Affiliations

3 authors, click to expand affiliations / ORCID

Sandhoff K

Andreae U

Jatzkewitz H

Article Info

Journal

Life sciences

Abbr.

Life Sci

ISSN

0024-3205

DOI

10.1016/0024-3205(68)90024-6

Published

1968-03-15

Pages

283-8

Language

English

Region

Netherlands

NLM ID

0375521

Subset

External Links

PubMed source DOI: 10.1016/0024-3205(68)90024-6 View journal details

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Deficient hexozaminidase activity in an exceptional case of Tay-Sachs disease with additional storage of kidney globoside in visceral organs.

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