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Frank Weidemann et al.
Journal of the American Society of Nephrology : JASN, 25(4), 837-849 (2014-02-22)
Because of the shortage of agalsidase-beta in 2009, many patients with Fabry disease were treated with lower doses or were switched to agalsidase-alfa. This observational study assessed end-organ damage and clinical symptoms during dose reduction or switch to agalsidase-alfa. A
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