Distinct amyloid fibril structures formed by ALS-causing SOD1 mutants G93A and D101N
Abstract Two hundred eight genetic mutations in SOD1 have been linked to amyotrophic lateral sclerosis (ALS). Of these, the G93A and D101N variants maintain much of their physiological function, closely resembling that of wild-type SOD1, and the SOD1-G93A transgenic mouse is the most extensively use...
Na minha lista:
| Principais autores: | , , , , , , , , , , , |
|---|---|
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Springer Nature
2025-08-01
|
| Serier: | EMBO Reports |
| Fag: | |
| Online adgang: | https://doi.org/10.1038/s44319-025-00557-8 |
| Tags: |
Ingen Tags, Vær først til at tagge denne postø!
|
