1989-03-01
Glycogenosis type II : a study on clinical heterogeneity and enzyme replacement therapy
Publication
Publication
Glycogenose type II : een studie met betrekking tot klinische heterogeniteit en enzymvervangingstherapie
Glycogenosis type II is a lysosomal storage disorder caused by deficiency of acid a-glucosidase and characterized by heart failure and skeletal muscle weakness. The experimental work described in this thesis was performed to elucidate the cause of clinical heterogeneity in this disease and to test the feasibility of receptor mediated enzyme replacement therapy.
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| , , , , , , | |
| Erasmus University Rotterdam | |
| H. Galjaard (Hans) | |
| hdl.handle.net/1765/50990 | |
| Organisation | Erasmus MC: University Medical Center Rotterdam |
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van der Ploeg, A. (1989, March). Glycogenosis type II : a study on clinical heterogeneity and enzyme replacement therapy. Retrieved from http://hdl.handle.net/1765/50990 |
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