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This suggested that this polysccharide accumulation occurred because the polysaccharide was laid down in a non 7hyphen;bioavailable form. The clinical and histochemical features in this patient and in the few similar reported cases indicate that polysaccharide storage myopathy is a distinct entity that is allied to the glycogen storage myopathies.<\/jats:p>","DOI":"10.1002\/mus.880110411","type":"journal-article","created":{"date-parts":[[2005,1,1]],"date-time":"2005-01-01T05:14:15Z","timestamp":1104556455000},"page":"349-355","source":"Crossref","is-referenced-by-count":21,"title":["Polysaccharide storage myopathy"],"prefix":"10.1002","volume":"11","author":[{"given":"A. J.","family":"Thompson","sequence":"first","affiliation":[]},{"given":"M.","family":"Swash","sequence":"additional","affiliation":[]},{"given":"E. L.","family":"Cox","sequence":"additional","affiliation":[]},{"given":"D. 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