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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Dades bibliogràfiques
Publicat a:Mol Pain
Autors principals: Weissmann, Carina, Albanese, Adriana A, Contreras, Natalia E, Gobetto, María N, Castellanos, Libia C Salinas, Uchitel, Osvaldo D
Format: Artigo
Idioma:Inglês
Publicat: SAGE Publications 2021
Matèries:
Review
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC8299890/
https://ncbi.nlm.nih.gov/pubmed/34284652
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/17448069211033172
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