Fabry Cardiomyopathy: Current Practice and Future Directions

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,...

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Detalles Bibliográficos
Autores principales: Yim, Jeffrey, Yau, Olivia, Yeung, Darwin F., Tsang, Teresa S. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8233708/
https://www.ncbi.nlm.nih.gov/pubmed/34204530
http://dx.doi.org/10.3390/cells10061532

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8233708/
https://www.ncbi.nlm.nih.gov/pubmed/34204530
http://dx.doi.org/10.3390/cells10061532

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