The characterization of a murine model of mucopolysaccharidosis II (Hunter syndrome)
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/s10545-007-0641-8
Reference18 articles.
1. Birkenmeier EH, Davisson MT, Beamer WG, et al (1989) Murine mucopolysaccharidosis type VII. Characterization of a mouse with beta-glucuronidase deficiency. J Clin Invest 83: 1258-266.
2. Cardone M, Polito VA, Pepe S, et al (2006) Correction of Hunter syndrome in the MPSII mouse model by AAV2/8-mediated gene delivery. Hum Mol Genet 15: 1225-236.
3. Clarke LA, Russell CS, Pownall S, et al (1997) Murine mucopolysaccharidosis type I: targeted disruption of the murine alpha-l-iduronidase gene. Hum Mol Genet 6: 503-11.
4. de Jong JGN, Wevers RA, Laarakkers C, Poorthuis BJ (1989) Dimethylmethylene blue-based spectrophotometry of glycosaminoglycans in untreated urine: a rapid screening procedure for mucopolysaccharidoses. Clin Chem 35: 1472-477.
5. de Jong JG, Wevers RA, Liebrand-van SR (1992) Measuring urinary glycosaminoglycans in the presence of protein: an improved screening procedure for mucopolysaccharidoses based on dimethylmethylene blue. Clin Chem 38: 803-07.
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