Oxidative Stress and Cardiovascular-Renal Damage in Fabry Disease: Is There Room for a Pathophysiological Involvement?

Fabry disease is an X-linked lysosomal storage disease caused by mutations in the GLA gene that lead to a reduction or an absence of the enzyme α-galactosidase A, resulting in the progressive and multisystemic accumulation of globotriaosylceramide. Clinical manifestation varies from mild to severe,...

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Detalles Bibliográficos
Autores principales: Ravarotto, Verdiana, Simioni, Francesca, Carraro, Gianni, Bertoldi, Giovanni, Pagnin, Elisa, Calò, Lorenzo A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6262438/
https://www.ncbi.nlm.nih.gov/pubmed/30400144
http://dx.doi.org/10.3390/jcm7110409

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6262438/
https://www.ncbi.nlm.nih.gov/pubmed/30400144
http://dx.doi.org/10.3390/jcm7110409

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