Title : Biochemical, pathological, and skeletal improvement of mucopolysaccharidosis VI after gene transfer to liver but not to muscle.

Pub. Date : 2008 Jan

PMID : 17955027






4 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Mucopolysaccharidosis VI (MPS VI) is caused by deficient activity of arylsulfatase B (ARSB), resulting in intralysosomal storage of dermatan sulfate (DS) and multisystem disease without central nervous system involvement. Dermatan Sulfate arylsulfatase B Rattus norvegicus
2 Mucopolysaccharidosis VI (MPS VI) is caused by deficient activity of arylsulfatase B (ARSB), resulting in intralysosomal storage of dermatan sulfate (DS) and multisystem disease without central nervous system involvement. Dermatan Sulfate arylsulfatase B Rattus norvegicus
3 Mucopolysaccharidosis VI (MPS VI) is caused by deficient activity of arylsulfatase B (ARSB), resulting in intralysosomal storage of dermatan sulfate (DS) and multisystem disease without central nervous system involvement. Dermatan Sulfate arylsulfatase B Rattus norvegicus
4 Mucopolysaccharidosis VI (MPS VI) is caused by deficient activity of arylsulfatase B (ARSB), resulting in intralysosomal storage of dermatan sulfate (DS) and multisystem disease without central nervous system involvement. Dermatan Sulfate arylsulfatase B Rattus norvegicus