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Autor:
Viridiana Berstein, Eduardo M. Pirotzky, Hernán D. Taconelli, M. Gabriela Gobbi, Lara Beider, Natali D. Salgueiro, Laila Dome, Roberto A. Diez, Hugo Sotelo, Sabrina Coppola
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 41, Iss , Pp 101149- (2024)
Fabry disease is a rare X-linked lysosomal condition that leads to the accumulation of glycosphingolipids in various tissues, causing cellular dysfunction, tissue remodeling, progressive fibrosis, and organ failure. The disease results from a deficie
Externí odkaz:
https://doaj.org/article/33eb0b7f06064adfb5036e9be6455123
