The natural course of infantile Pompe's disease: 20 Original cases compared with 133 cases from the literature

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Keywords	α-glucosidase, Acid maltase, Enzyme replacement, Glycogen storage disease type II, Pompe's disease
Persistent URL	doi.org/10.1542/peds.112.2.332, hdl.handle.net/1765/63470
Journal	Pediatrics (English Edition)
Organisation	Department of Neurology
Citation APA APA Style APA-ALL Style AAA Style Cell Style Chicago Style Harvard Style IEEE Style MLA Style Nature Style Vancouver Style American-Institute-of-Physics Style Council-of-Science-Editors Style BibTex Format Endnote Format RIS Format CSL Format DOIs only Format	van den Hout, H., Hop, W., van Diggelen, O., Smeitink, J., Smit, G. P., Poll-The, B. T., Bakker, H., Loonen, C., de Klerk, J., Reuser, A.& van der Ploeg, A. (2003). The natural course of infantile Pompe's disease: 20 Original cases compared with 133 cases from the literature. Pediatrics (English Edition), 112(2 I), 332–340.https://doi.org/10.1542/peds.112.2.332

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