v1
Mutant huntingtin promotes the fibrillogenesis of wild-type huntingtin: a potential mechanism for loss of huntingtin function in Huntington's disease.
Identifier:nobleid.org/w1/20260515/DCF43C01
Type:Journal Article
0 views
Embeddable Badge
[](https://nobleid.org/work/w1/20260515/DCF43C01)
Bibliometric Analysis
Impact metrics, research fronts, co-authorship networks →
Authors & Claims