| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 11010890 | Molecular Genetics and Metabolism | 2018 | 47 Pages |
Abstract
In this review, we discuss the clinical symptoms of each MPS type as they initially appear in patients, biochemical and molecular diagnostic methods, and the future of newborn screening for this group of disorders.
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Authors
Molly Stapleton, Nivethitha Arunkumar, Francyne Kubaski, Robert W. Mason, Orii Tadao, Shunji Tomatsu,