Simultaneous absence of α-1,4-glucosidase and α-1,6-glucosidase activities (pH 4) in tissues of children with Type II glycogen storage disease

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Bibliographic Details
Published in:	Biochemistry (Easton) Vol. 9; no. 6; pp. 1423 - 1428
Main Authors:	Brown, Barbara Illingworth, Brown, David Henry, Jeffrey, Peter L
Format:	Journal Article
Language:	English
Published:	United States American Chemical Society 01-03-1970
Subjects:	Autopsy Biopsy Child Culture Techniques Disaccharides Drug Stability Fibroblasts - enzymology Glucosidases - antagonists & inhibitors Glucosidases - metabolism Glycogen Glycogen Storage Disease - enzymology Glycoside Hydrolases - metabolism Glycosides Humans Hydrogen-Ion Concentration Kinetics Leukocytes - enzymology Liver - enzymology Lysosomes - enzymology Maltose Muscles - enzymology Myocardium - enzymology
Online Access:	Get full text
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Bibliography:	istex:F028A1C1B0C350D58FA237FA27C65EE9592C0E65 ark:/67375/TPS-7V18T31N-R ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23
ISSN:	0006-2960 1520-4995
DOI:	10.1021/bi00808a017