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Effect of enzyme replacement therapy on bone formation in a feline model of mucopolysaccharidosis type VI

โœ Scribed by S. Byers; J.D. Nuttall; A.C. Crawley; J.J. Hopwood; K. Smith; N.L. Fazzalari

Book ID
118660917
Publisher
Elsevier Science
Year
1997
Tongue
English
Weight
870 KB
Volume
21
Category
Article
ISSN
8756-3282

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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