Structures of fibrils formed by α-synuclein hereditary disease mutant H50Q reveal new polymorphs
Author:
Publisher
Springer Science and Business Media LLC
Subject
Molecular Biology,Structural Biology
Link
http://www.nature.com/articles/s41594-019-0322-y.pdf
Reference51 articles.
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2. Grazia Spillantini, M. et al. Filamentous α-synuclein inclusions link multiple system atrophy with Parkinson’s disease and dementia with Lewy bodies. Neurosci. Lett. 251, 205–208 (1998).
3. Spillantini, M. G. & Goedert, M. Neurodegeneration and the ordered assembly of α-synuclein. Cell Tissue Res. 373, 137–148 (2018).
4. Singleton, A. B. et al. α-Synuclein locus triplication causes parkinson’s disease. Science 302, 841–841 (2003).
5. Chartier-Harlin, M.-C. et al. α-synuclein locus duplication as a cause of familial Parkinson’s disease. Lancet 364, 1167–1169 (2004).
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