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...

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Detalles Bibliográficos
Autores principales: Weissmann, Carina, Albanese, Adriana A, Contreras, Natalia E, Gobetto, María N, Castellanos, Libia C Salinas, Uchitel, Osvaldo D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Review
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

Internet

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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