An assay for iduronate sulfatase (Hunter corrective factor)
- PMID: 4214613
- DOI: 10.1016/s0008-6215(00)87067-6
An assay for iduronate sulfatase (Hunter corrective factor)
Similar articles
-
The defect in the Hunter syndrome: deficiency of sulfoiduronate sulfatase.Proc Natl Acad Sci U S A. 1973 Jul;70(7):2134-8. doi: 10.1073/pnas.70.7.2134. Proc Natl Acad Sci U S A. 1973. PMID: 4269173 Free PMC article.
-
Hunter's syndrome: a deficiency of L-idurono-sulfate sulfatase.Biochem Biophys Res Commun. 1973 Oct 1;54(3):1125-32. doi: 10.1016/0006-291x(73)90809-7. Biochem Biophys Res Commun. 1973. PMID: 4270969 No abstract available.
-
Radioactive substrates for iduronate sulfatase and alpha-L-iduronidase.Methods Enzymol. 1978;50:150-4. doi: 10.1016/0076-6879(78)50013-x. Methods Enzymol. 1978. PMID: 661572 No abstract available.
-
Iduronate sulfatase analysis of hair roots for identification of Hunter syndrome heterozygotes.Am J Hum Genet. 1978 Nov;30(6):575-82. Am J Hum Genet. 1978. PMID: 106723 Free PMC article.
-
Idursulfase in Hunter syndrome treatment.Drugs Today (Barc). 2007 Nov;43(11):759-67. doi: 10.1358/dot.2007.43.11.1157619. Drugs Today (Barc). 2007. PMID: 18174963 Review.
Cited by
-
Mosaicism for sulfoiduronate sulfatase deficiency in carriers of Hunter's syndrome.Experientia. 1976 Apr 15;32(4):459-60. doi: 10.1007/BF01920795. Experientia. 1976. PMID: 817929
-
Functional assessment of the genetic findings indicating mucopolysaccharidosis type II in the prenatal setting.JIMD Rep. 2021 Mar 26;60(1):10-14. doi: 10.1002/jmd2.12214. eCollection 2021 Jul. JIMD Rep. 2021. PMID: 34258136 Free PMC article.
-
Human liver glucuronate 2-sulphatase. Purification, characterization and catalytic properties.Biochem J. 1989 Apr 1;259(1):209-16. doi: 10.1042/bj2590209. Biochem J. 1989. PMID: 2497731 Free PMC article.
-
The mucopolysaccharidoses (a review).Proc Natl Acad Sci U S A. 1976 Feb;73(2):630-7. doi: 10.1073/pnas.73.2.630. Proc Natl Acad Sci U S A. 1976. PMID: 813230 Free PMC article.
-
Normal excretion of urinary acid mucopolysaccharides in a boy with iduronate sulphatase deficiency, Hunter phenotype and alpha 1-antitrypsin deficiency.Eur J Pediatr. 1986 Dec;145(6):572-5. doi: 10.1007/BF02429071. Eur J Pediatr. 1986. PMID: 2949978
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources