Alpha 2.0
Login Register
» Articles » PMID: 5273538

The Fine Structure of Glycogen from Type IV Glycogen-storage Disease

Overview
Journal Eur J Biochem
Specialty Biochemistry
Date 1970 Nov 1
PMID 5273538
Citations 6
Authors
C Mercier
W J WHELAN
Affiliations
Soon will be listed here.
Citing Articles

A Modified Enzymatic Method for Measurement of Glycogen Content in Glycogen Storage Disease Type IV.

Yi H, Zhang Q, Yang C, Kishnani P, Sun B JIMD Rep. 2016; 30:89-94.

PMID: 27344645 PMC: 5110445. DOI: 10.1007/8904_2015_522.

How did glycogen structure evolve to satisfy the requirement for rapid mobilization of glucose? A problem of physical constraints in structure building.

Melendez R, Cascante M J Mol Evol. 1997; 45(4):446-55.

PMID: 9321423 DOI: 10.1007/pl00006249.

Juvenile hereditary polyglucosan body disease with complete branching enzyme deficiency (type IV glycogenosis).

Schroder J, May R, Shin Y, Sigmund M Acta Neuropathol. 1993; 85(4):419-30.

PMID: 7683169 DOI: 10.1007/BF00334454.

Light and electron microscopy of skeletal muscle in type IV glycogenosis.

SCHOCHET Jr S, MCCORMICK W, Kovarsky J Acta Neuropathol. 1971; 19(2):137-44.

PMID: 5288587 DOI: 10.1007/BF00688492.

Enzymic explorations of the structures of starch and glycogen.

WHELAN W Biochem J. 1971; 122(5):609-22.

PMID: 5001952 PMC: 1176828. DOI: 10.1042/bj1220609.