Eun-Jong Lee

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BACKGROUND/AIMS Fabry disease is an X-linked recessive and progressive disease caused by α-galactosidase A (α-GaL A) deficiency. We sought to assess the prevalence of unrecognized Fabry disease in dialysis-dependent patients and the efficacy of serum globotriaosylceramide (GL3) screening. METHODS A total of 480 patients of 1,230 patients among 17 clinics(More)
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