Anderson–Fabry Disease: A New Piece of the Lysosomal Puzzle in Parkinson Disease?

Anderson–Fabry disease (AFD) is an inherited lysosomal storage disorder characterized by a composite and multisystemic clinical phenotype and frequent involvement of the central nervous system (CNS). Research in this area has largely focused on the cerebrovascular manifestations of the disease, and...

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Detalles Bibliográficos
Autores principales: Zedde, Marialuisa, Pascarella, Rosario, Cavallieri, Francesco, Pezzella, Francesca Romana, Grisanti, Sara, Di Fonzo, Alessio, Valzania, Franco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9776280/
https://www.ncbi.nlm.nih.gov/pubmed/36551888
http://dx.doi.org/10.3390/biomedicines10123132

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9776280/
https://www.ncbi.nlm.nih.gov/pubmed/36551888
http://dx.doi.org/10.3390/biomedicines10123132

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