The Childhood-Onset Neurodegeneration with Cerebellar Atrophy (CONDCA) Disease Caused by AGTPBP1 Gene Mutations: The Purkinje Cell Degeneration Mouse as an Animal Model for the Study of this Human Disease

Recent reports have identified rare, biallelic damaging variants of the AGTPBP1 gene that cause a novel and documented human disease known as childhood-onset neurodegeneration with cerebellar atrophy (CONDCA), linking loss of function of the AGTPBP1 protein to human neurodegenerative diseases. CONDC...

Descripción completa

Detalles Bibliográficos
Autores principales: Baltanás, Fernando C., Berciano, María T., Santos, Eugenio, Lafarga, Miguel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8464709/
https://www.ncbi.nlm.nih.gov/pubmed/34572343
http://dx.doi.org/10.3390/biomedicines9091157

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8464709/
https://www.ncbi.nlm.nih.gov/pubmed/34572343
http://dx.doi.org/10.3390/biomedicines9091157

Ejemplares similares