Fabry Cardiomyopathy: Current Practice and Future Directions
Fabry Cardiomyopathy: Current Practice and Future Directions
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Publisher
Basel: MDPI AG
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Language
English
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Publisher
Basel: MDPI AG
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Contents
Fabry disease (FD) is an X-linked lysosomal storage disorder caused by mutations in the galactosidase A (GLA) gene that result in deficient galactosidase A enzyme and subsequent accumulation of glycosphingolipids throughout the body. The result is a multi-system disorder characterized by cutaneous, corneal, cardiac, renal, and neurological manifest...
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Full title
Fabry Cardiomyopathy: Current Practice and Future Directions
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TN_cdi_doaj_primary_oai_doaj_org_article_e5beb874f291423db3ac4d4ade4d1230
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_e5beb874f291423db3ac4d4ade4d1230
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ISSN
2073-4409
E-ISSN
2073-4409
DOI
10.3390/cells10061532
