Arrhythmogenesis in Fabry Disease
<p><strong>Purpose of Review</p></strong> Fabry Disease (FD) is a rare lysosomal storage disorder characterised by multiorgan accumulation of glycosphingolipid due to deficiency in the enzyme α-galactosidase A. Cardiac sphingolipid accumulation triggers various types of arr...
Main Authors: | Roy, A, Cumberland, MJ, O'Shea, C, Holmes, A, Kalla, M, Gehmlich, K, Geberhiwot, T, Steeds, RP |
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Format: | Journal article |
Language: | English |
Published: |
Springer Nature
2024
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