α-1,4-Glucosidase Activity in Leucocytes from the Family of Two Brothers Who Lack this Enzyme in Muscle
- 1 October 1966
- journal article
- Published by Portland Press Ltd. in Biochemical Journal
- Vol. 101 (1), 16C
- https://doi.org/10.1042/bj1010016c
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- [Muscular glycogenosis caused by alpha-1,4-glucosidase deficiency simulating progressive muscular dystrophy. (Clinical and enzyme study. Optic and electron microscopy)].1965
- Glycogen storage diseaseAmerican Journal Of Medicine, 1965
- A MILD FORM OF MUSCULAR GLYCOGENOSIS IN 2 BROTHERS WITH ALPHA-1,4-GLUCOSIDASE DEFICIENCY1965
- The subcellular distribution of enzymes in type II glycogenosis and the occurrence of an oligo-α-1,4-glucan glucohydrolase in human tissuesBiochimica et Biophysica Acta (BBA) - Enzymology and Biological Oxidation, 1965
- Generalized glycogenosis: Report of a case with deficiency of alpha glucosidaseThe Journal of Pediatrics, 1964
- Amylo-1,6-glucosidase activity in normal leucocytes and in leucocytes of patients with glycogen-storage diseaseClinica Chimica Acta; International Journal of Clinical Chemistry, 1964
- ELECTRON MICROSCOPIC + BIOCHEMICAL STUDY OF TYPE 2 GLYCOGENOSIS1964
- Diagnosis of generalized glycogen storage disease (Pompe's disease)The Journal of Pediatrics, 1963
- α-Glucosidase deficiency in generalized glycogen-storage disease (Pompe's disease)Biochemical Journal, 1963