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Anderson-Fabry disease is a rare X-linked lysosomal storage disorder due to the deficiency of alfa-galactosidase A (AGAL). The subsequent accumulation of glycosphingolipids may lead to to cardiac, ren...
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Lead Sponsor
Klinikum Wels-Grieskirchen
Collaborators
Klinikum Wels-Grieskirchen
Wels, Upper Austria
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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