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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...
में बचाया:
| में प्रकाशित: | Front Cardiovasc Med |
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| मुख्य लेखक: | |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
Frontiers Media S.A.
2016
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4805598/ https://ncbi.nlm.nih.gov/pubmed/27047943 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fcvm.2016.00007 |
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