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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Dades bibliogràfiques
Publicat a:J Clin Med
Autors principals: Ravarotto, Verdiana, Simioni, Francesca, Carraro, Gianni, Bertoldi, Giovanni, Pagnin, Elisa, Calò, Lorenzo A.
Format: Artigo
Idioma:Inglês
Publicat: MDPI 2018
Matèries:
Review
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6262438/
https://ncbi.nlm.nih.gov/pubmed/30400144
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/jcm7110409
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