Mucopolysaccharidosis type VI (MPS VI) or Maroteaux-Lamy syndrome, is a autosomal recessive disorder, due to the deficiency of the lysosomal enzyme N-acetylgalactosamine-4-sulfatase (arylsulfatase B, ASB: EC 3.1.6.12). Three classical forms of the disease have been differentiated: severe, intermedia
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Four novel mutant alleles of the arylsulfatase B gene in two patients with intermediate form of mucopolysaccharidosis VI (Maroteaux-Lamy syndrome)
β Scribed by Elena Voskoboeva; Dirk Isbrandt; Kurt Figura; Xenia Krasnopolskaya; Christoph Peters
- Book ID
- 104666898
- Publisher
- Springer
- Year
- 1994
- Tongue
- English
- Weight
- 821 KB
- Volume
- 93
- Category
- Article
- ISSN
- 0340-6717
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