Modeling the effect of enzyme replacement therapy on life-threatening complications in patients with Fabry disease
Fabry disease (FD) is a severe lysosome storage disease caused by congenital deficiency of the enzyme α-galactosidase A and characterized by the risk of renal failure combined with cardiovascular and CNS complications. According to the currently available information, the early start of enzyme repla...
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IRBIS LLC,
2019-01-01T00:00:00Z.
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