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Ion channels and pain in Fabry disease
Fabry disease (FD) is a progressive, X-linked inherited disorder of glycosphingolipid metabolism due to deficient or absent lysosomal α-galactosidase A (α-Gal A) activity which results in progressive accumulation of globotriaosylceramide (Gb3) and related metabolites. One prominent feature of Fabry...
Autores principales: | Weissmann, Carina, Albanese, Adriana A, Contreras, Natalia E, Gobetto, María N, Castellanos, Libia C Salinas, Uchitel, Osvaldo D |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8299890/ https://www.ncbi.nlm.nih.gov/pubmed/34284652 http://dx.doi.org/10.1177/17448069211033172 |
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