Mutant VAPB: Culprit or Innocent Bystander of Amyotrophic Lateral Sclerosis?

Nearly twenty years ago a mutation in the VAPB gene, resulting in a proline to serine substitution (p.P56S), was identified as the cause of a rare, slowly progressing, familial form of the motor neuron degenerative disease Amyotrophic Lateral Sclerosis (ALS). Since then, progress in unravelling the...

Descripción completa

Detalles Bibliográficos
Autores principales: Borgese, Nica, Navone, Francesca, Nukina, Nobuyuki, Yamanaka, Tomoyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10243577/
https://www.ncbi.nlm.nih.gov/pubmed/37366377
http://dx.doi.org/10.1177/25152564211022515

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10243577/
https://www.ncbi.nlm.nih.gov/pubmed/37366377
http://dx.doi.org/10.1177/25152564211022515

Ejemplares similares