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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Veröffentlicht in:	Biochemistry (Easton) 1970-03, Vol.9 (6), p.1423-1428
Hauptverfasser:	Brown, Barbara Illingworth, Brown, David Henry, Jeffrey, Peter L
Format:	Artikel
Sprache:	eng
Schlagworte:	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
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