Neurometabolic Dysfunction in SPG11 Hereditary Spastic Paraplegia

Background: Pathogenic variants in SPG11 cause the most common autosomal recessive complicated hereditary spastic paraplegia. Besides the prototypical combination of spastic paraplegia with a thin corpus callosum, obesity has increasingly been reported in this multisystem neurodegenerative disease....

Descripción completa

Detalles Bibliográficos
Autores principales: Regensburger, Martin, Krumm, Laura, Schmidt, Manuel Alexander, Schmid, Andreas, Spatz, Imke Tabea, Marterstock, Dominique Cornelius, Kopp, Christoph, Kohl, Zacharias, Doerfler, Arnd, Karrasch, Thomas, Winner, Beate, Winkler, Jürgen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9693816/
https://www.ncbi.nlm.nih.gov/pubmed/36432490
http://dx.doi.org/10.3390/nu14224803

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9693816/
https://www.ncbi.nlm.nih.gov/pubmed/36432490
http://dx.doi.org/10.3390/nu14224803

Ejemplares similares