Review of the use of idursulfase in the treatment of mucopolysaccharidosis II

Mucopolysaccharidosis type II (MPS II, Hunter syndrome) is a heterogeneous, progressive X-linked recessively inherited lysosomal storage disease that is caused by a deficiency of the enzyme iduronate-2-sulfatase, resulting in abnormal tissue accumulation of the glycosaminoglycans, dermatan sulfate a...

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Detalles Bibliográficos
Autores principales: Burrow, T Andrew, Leslie, Nancy D
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2008
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2721351/
https://www.ncbi.nlm.nih.gov/pubmed/19707363

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2721351/
https://www.ncbi.nlm.nih.gov/pubmed/19707363

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