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Cardiac manifestations in patients with classical or cardiac subtype of Fabry disease
BACKGROUND: Fabry disease (FD) is an X-linked lysosomal storage disorder engendered by a deficiency of the enzyme α-galactosidase A, leading to systemic accumulation of glycolipids. Studies have reported that the cardiac subtype of FD has a later onset and minimal extracardiac involvement. However,...
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| Publicado no: | J Chin Med Assoc |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Lippincott Williams & Wilkins
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7478196/ https://ncbi.nlm.nih.gov/pubmed/32649415 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/JCMA.0000000000000379 |
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