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alpha-Glucosidase deficiency (Pompe's disease)
J. M. Tager
,
R. P. Oude Elferink
, A. Reuser
, M. Kroos
, L. A. Ginsel
, J. A. Fransen
, J. Klumperman
Other Departments
Affiliatie UvA
Research output
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peer-review
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Keyphrases
α-glucosidase
100%
Pompe Disease
100%
Clinical Symptoms
25%
Phosphorylation
25%
Kidney
25%
Small Intestine
25%
Clinical Phenotype
25%
Brush Border
25%
Defect Type
25%
Polarized Epithelial Cells
25%
Medicine and Dentistry
Precursor
100%
Glycogen Storage Disease Type II
100%
Alpha Glucosidase
100%
Small Intestine
20%
Messenger RNA
20%
Epithelial Cell
20%
Brush Border
20%
Biochemistry, Genetics and Molecular Biology
Precursor
100%
Alpha-Glucosidase
100%
Enzyme
40%
Messenger RNA
20%
Small Intestine
20%
Brush Border
20%
Immunology and Microbiology
Precursor
100%
Glucosidase
100%
Small Intestine
20%
Brush Border
20%
Pharmacology, Toxicology and Pharmaceutical Science
Glycogen Storage Disease Type 2
100%
Alpha Glucosidase
100%
Messenger RNA
25%