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Electrocardiographic Changes and Arrhythmia in Fabry Disease
Fabry disease is an X-chromosome-linked lysosomal storage disease characterized by a deficient activity or, in most males, absence of the enzyme α-galactosidase A (a-Gal A) leading to systemic, primary lysosomal accumulation of globotriaosylceramide (Gb3) (1). Recent literature refers to an overall...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Frontiers Media S.A.
2016
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4805598/ https://www.ncbi.nlm.nih.gov/pubmed/27047943 http://dx.doi.org/10.3389/fcvm.2016.00007 |