Fabry Disease and the Heart: A Comprehensive Review

Fabry disease (FD) is an X-linked lysosomal storage disorder caused by mutations of the GLA gene that result in a deficiency of the enzymatic activity of α-galactosidase A and consequent accumulation of glycosphingolipids in body fluids and lysosomes of the cells throughout the body. GB3 accumulatio...

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Detalles Bibliográficos
Autores principales: Azevedo, Olga, Cordeiro, Filipa, Gago, Miguel Fernandes, Miltenberger-Miltenyi, Gabriel, Ferreira, Catarina, Sousa, Nuno, Cunha, Damião
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8123068/
https://www.ncbi.nlm.nih.gov/pubmed/33922740
http://dx.doi.org/10.3390/ijms22094434

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8123068/
https://www.ncbi.nlm.nih.gov/pubmed/33922740
http://dx.doi.org/10.3390/ijms22094434

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