## ABSTRACT Fabry disease is a multisystem disorder associated with wide variability in clinical expression. Fabry disease is an Xโlinked lysosomal storage disorder caused by a deficiency of ฮฑโgalactosidaseย A. The enzyme defect leads to the systemic accumulation of glycosphingolipids with ฮฑโgalacto
โฆ LIBER โฆ
Clinical benefit of enzyme replacement therapy in Fabry disease
โ Scribed by Breunig, F; Weidemann, F; Strotmann, J; Knoll, A; Wanner, C
- Book ID
- 110052598
- Publisher
- Nature Publishing Group
- Year
- 2006
- Tongue
- English
- Weight
- 113 KB
- Volume
- 69
- Category
- Article
- ISSN
- 0085-2538
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