A novel hotspot of gelsolin instability triggers an alternative mechanism of amyloid aggregation
Gelsolin comprises six homologous domains, named G1 to G6. Single point substitutions in this protein are responsible for AGel amyloidosis, a hereditary disease causing progressive corneal lattice dystrophy, cutis laxa, and polyneuropathy. Although several different amyloidogenic variants of gelsoli...
Saved in:
| Main Authors: | , , , , , , , , , , , , , , , , |
|---|---|
| Format: | article |
| Language: | EN |
| Published: |
Elsevier
2021
|
| Subjects: | |
| Online Access: | https://doaj.org/article/28c0fa7cd36a48168031138ec41efe6d |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|