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Lancet, The, ISSN 0140-6736, 2012, Volume 379, Issue 9813, pp. 335 - 341
Journal Article
Genetics in Medicine, ISSN 1098-3600, 05/2006, Volume 8, Issue 5, pp. 267 - 288
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Clinical Chemistry, ISSN 0009-9147, 09/2013, Volume 59, Issue 9, pp. 1357 - 1368
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Journal of Neurology, Neurosurgery and Psychiatry, ISSN 0022-3050, 01/2016, Volume 87, Issue 1, pp. 5 - 11
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Orphanet journal of rare diseases, ISSN 1750-1172, 2012, Volume 7, Issue 1, pp. 88 - 88
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Neurology, ISSN 0028-3878, 03/2016, Volume 86, Issue 13, pp. 1260 - 1261
Classic infantile Pompe disease is a progressive lysosomal glycogen storage disorder, which, if untreated, leads to severe skeletal muscle weakness, inability... 
ENZYME REPLACEMENT THERAPY | CLINICAL NEUROLOGY | Cognition Disorders - diagnosis | Cognition Disorders - complications | Glycogen Storage Disease Type II - complications | Humans | Male | Glycogen Storage Disease Type II - diagnosis | Child | Index Medicus | Abridged Index Medicus
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