Enzyme replacement therapy with idursulfase in patients with mucopolysaccharidosis type II
Author:
Publisher
Wiley
Subject
General Medicine,Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1651-2227.2008.00661.x/fullpdf
Reference16 articles.
1. Cumulative incidence rates of the mucopolysaccharidoses in Germany
2. The frequency of lysosomal storage diseases in The Netherlands
3. A clinical study of 77 patients with mucopolysaccharidosis type II
4. A clinical and genetic study of Hunter's syndrome. 1 Heterogeneity
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