A fluorimetric enzyme assay for the diagnosis of MPS II (hunter disease)

Journal of Inherited Metabolic Disease

Volumn 24, Issue 6, 2001, Pages 675-680

  Voznyi, Ya V ^a   Keulemans, J L M ^b   Van Diggelen, O P ^b  

^a Technology of Hetero organic Compounds   (Russian Federation)

^b ERASMUS UNIVERSITY ROTTERDAM   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

4 METHYLUMBELLIFERYL ALPHA IDURONATE 2 SULFATE; DIAGNOSTIC AGENT; FLUOROCHROME; HYMECROMONE SULFATE; IDURONATE 2 SULFATASE; LEVO IDURONIDASE; UNCLASSIFIED DRUG;

ARTICLE; CONTROLLED STUDY; ENZYME ACTIVITY; ENZYME ASSAY; ENZYME PURIFICATION; ENZYME SUBSTRATE; FIBROBLAST; FLUOROMETRY; HUMAN; HUMAN CELL; HUNTER SYNDROME; HYDROLYSIS; INCUBATION TIME; LEUKOCYTE; LYSOSOME; PLASMA; SYNTHESIS;

FIBROBLASTS; FLUOROMETRY; HUMANS; HYDROGEN-ION CONCENTRATION; HYMECROMONE; IDURONATE SULFATASE; IDURONIC ACID; LEUKOCYTES; LYSOSOMES; MUCOPOLYSACCHARIDOSIS II; SUBSTRATE SPECIFICITY;

EID: 0035194407     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1012763026526     Document Type: Article

References (7)

1. The defect in the Hunter syndrome: Deficiency of sulfoiduronate sulfatase
2. Enzymatic diagnosis of the genetic mucopolysaccharide storage disorders
3. α-L-iduronidase, β-D-glucuronidase, and 2-sulfo-L-iduronate 2-sulfatase: Preparation and characterisation of radioactive substrates from heparin
4. The mucopolysaccharidoses
5. 1
6. A fluorimetric enzyme assay for the diagnosis of Morquio disease type A (MPS IV A)
7. Purification of acid β-galactosidase and acid neuraminidase from bovine testis: Evidence for an enzyme complex