Presentation and treatments for Mucopolysaccharidosis Type II (MPS II; Hunter Syndrome)-Reference-Cited by-同舟云学术

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Presentation and treatments for Mucopolysaccharidosis Type II (MPS II; Hunter Syndrome)

Published:2017-03-08 Issue:4 Volume:5 Page:295-307
ISSN:2167-8707
Container-title:Expert Opinion on Orphan Drugs
language:en
Short-container-title:Expert Opinion on Orphan Drugs

Author:

Stapleton Molly¹²,Kubaski Francyne¹²,Mason Robert W.¹²,Yabe Hiromasa³,Suzuki Yasuyuki⁴,Orii Kenji E.⁵,Orii Tadao⁵,Tomatsu Shunji¹²⁵

Affiliation:

1. Department of Biological Sciences, University of Delaware, Newark, DE, USA

2. Department of Skeletal Dysplasia, Nemours/Alfred I. duPont Hospital for Children, Wilmington, DE, USA

3. Department of Cell Transplantation and Regenerative Medicine, Tokai University School of Medicine, Isehara, Japan

4. Medical Education Development Center, Gifu University, Gifu, Japan

5. Department of Pediatrics, Graduate School of Medicine, Gifu University, Gifu, Japan

Funder

NIH Clinical Center

Publisher

Informa UK Limited

Subject

Pharmacology (medical),Health Policy,Pharmacology, Toxicology and Pharmaceutics (miscellaneous)

Link

https://www.tandfonline.com/doi/pdf/10.1080/21678707.2017.1296761

Reference160 articles.

1. Gargoylism – A mucopolysaccharidosis

2. Inborn Errors of Mucopolysaccharide Metabolism

3. The Defect in the Hunter Syndrome: Deficiency of Sulfoiduronate Sulfatase

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