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Plasmatic kinetics of dermatan sulfate during enzyme replacement therapy with iduronate-2-sulfatase in a mucopolysaccharidosis II Patient

✍ Scribed by Volpi, Nicola; Zampini, Lucia; Maccari, Francesca; Santoro, Lucia; Galeotti, Fabio; Galeazzi, Tiziana; Gabrielli, Orazio; Coppa, Giovanni V.


Book ID
125360628
Publisher
Springer US
Year
2013
Tongue
English
Weight
184 KB
Volume
30
Category
Article
ISSN
1573-4986

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## Communicated by David N. Cooper Various types of complex genetic rearrangements involving the iduronate-2-sulfatase (IDS) and its homologous pseudogene (IDS2, IDSP1) have so far been reported as the cause of Mucopolysaccharidosis type II (MPS2 or MPS II; Hunter syndrome). When using conventiona