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Enzyme replacement therapy for Fabry's disease

✍ Scribed by Patrick Deegan


Book ID
117306641
Publisher
The Lancet
Year
2010
Tongue
English
Weight
91 KB
Volume
375
Category
Article
ISSN
0140-6736

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## ABSTRACT Fabry disease is a multisystem disorder associated with wide variability in clinical expression. Fabry disease is an X‐linked lysosomal storage disorder caused by a deficiency of α‐galactosidaseΒ A. The enzyme defect leads to the systemic accumulation of glycosphingolipids with α‐galacto

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