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Infantile neuroaxonal dystrophy: Axonal changes in biopsied muscle tissue

✍ Scribed by Wakai, Shuji; Asanuma, Hideomi; Tachi, Nobutada; Ishikawa, Yukitoshi; Minami, Ryoji


Book ID
122879004
Publisher
Elsevier Science
Year
1993
Tongue
English
Weight
594 KB
Volume
9
Category
Article
ISSN
0887-8994

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## Abstract Pompe's disease (glycogen storage disease type II) is an autosomal recessive myopathy caused by lysosomal α‐glucosidase deficiency. Enzyme replacement therapy (ERT) is currently under development for this disease. We evaluated the morphological changes in muscle tissue of four children