Glycosphingolipids and their impact on platelet activity in a murine model of fabry disease
Glycosphingolipids and their impact on platelet activity in a murine model of fabry disease
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London: Nature Publishing Group UK
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English
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London: Nature Publishing Group UK
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Fabry disease is an X-linked lysosomal storage disorder caused by deficiency of the lysosomal enzyme ⍺-galactosidase-A (⍺-Gal A), resulting in widespread accumulation of terminal galactose-containing glycosphingolipids (GSLs) and the impairment of multiple organ systems. Thrombotic events are common in Fabry patients, with strokes and heart attacks...
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Glycosphingolipids and their impact on platelet activity in a murine model of fabry disease
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TN_cdi_doaj_primary_oai_doaj_org_article_39a61f23e43a431bb7f1fc26b70a1766
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_39a61f23e43a431bb7f1fc26b70a1766
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ISSN
2045-2322
E-ISSN
2045-2322
DOI
10.1038/s41598-024-80633-6
