Deficiency of glucosylsphingosine: beta-glucosidase in Gaucher disease.

Biochemical and biophysical research communications ·Vol. 54 ·No. 1 ·1973-09-05 ·Pages 256-63

Raghavan SS, Mumford RA, Kanfer JN

Abstract

暂无摘要

MeSH Terms

Adult Carbon Radioisotopes Cells, Cultured Child Chromatography, Thin Layer Diffuse Cerebral Sclerosis of Schilder/enzymology Female Fibroblasts/enzymology Gaucher Disease/enzymology Glucosidases/metabolism Glycosides/analysis Heart Defects, Congenital/enzymology Heart Diseases/enzymology Hexosaminidases/metabolism Humans Infant Infant, Newborn Male Middle Aged Niemann-Pick Diseases/enzymology Skin/enzymology Sphingosine/analysis Spleen/analysis,enzymology

Chemicals

Carbon Radioisotopes Glycosides Glucosidases Hexosaminidases Sphingosine

Authors & Affiliations

3 authors, click to expand affiliations / ORCID

Raghavan S S

Mumford R A

Kanfer J N

Article Info

Journal

Biochemical and biophysical research communications

Abbr.

Biochem Biophys Res Commun

ISSN

0006-291X

DOI

10.1016/0006-291x(73)90916-9

Published

1973-09-05

Pages

256-63

Language

English

Region

United States

NLM ID

0372516

Subset

External Links

PubMed source DOI: 10.1016/0006-291x(73)90916-9 View journal details

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Deficiency of glucosylsphingosine: beta-glucosidase in Gaucher disease.

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