A new substrate for the detection of amylo-1,6-glucosidase, and its application to the study of glycogen-storage disease type 3

Arch Biochem Biophys. 1966 Feb;113(2):500-2. doi: 10.1016/0003-9861(66)90221-9.

Authors

P M Taylor, W J Whelan

PMID: 5221002
DOI: 10.1016/0003-9861(66)90221-9

No abstract available

MeSH terms

Glycogen Storage Disease*
Glycoside Hydrolases*
Humans
In Vitro Techniques
Liver / enzymology
Muscles / enzymology
Polysaccharides*
Subcellular Fractions

Substances

Polysaccharides
Glycoside Hydrolases