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P464: Electroencephalographic evaluation of mucopolysaccharidosis type II undergoing enzyme replacement therapy

✍ Scribed by Kinoshita, M.; Furujo, M.; Kubo, T.

Book ID
125803771
Publisher
Elsevier Science
Year
2014
Tongue
English
Weight
63 KB
Volume
125
Category
Article
ISSN
1388-2457

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## Communicated by Andreas Gal Mucopolysaccharidosis type VI (MPS VI), or Maroteaux-Lamy syndrome, is a lysosomal storage disorder caused by a deficiency of N-acetylgalactosamine-4-sulfatase (ARSB). Seven MPS VI patients were chosen for the initial clinical trial of enzyme replacement therapy. Dir