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 |
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container_title | Biochemistry (Easton) |
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creator | Brown, Barbara Illingworth Brown, David Henry Jeffrey, Peter L |
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doi_str_mv | 10.1021/bi00808a017 |
format | Article |
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language | eng |
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source | ACS Publications; MEDLINE |
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 |
title | 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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