Parkinson disease genetics: too early to predict progression?
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Neurology (clinical)
Link
http://www.nature.com/articles/s41582-019-0264-3.pdf
Reference10 articles.
1. Polymeropoulos, M. H. et al. Mutation in the alpha-synuclein gene identified in families with Parkinson’s disease. Science 276, 2045–2047 (1997).
2. Brockmann, K. et al. GBA-associated PD presents with nonmotor characteristics. Neurology 77, 276–280 (2011).
3. Brockmann, K. et al. GBA-associated Parkinson’s disease: reduced survival and more rapid progression in a prospective longitudinal study. Mov. Disord. 30, 407–411 (2015).
4. Winder-Rhodes, S. E. et al. Glucocerebrosidase mutations influence the natural history of Parkinson’s disease in a community-based incident cohort. Brain 136, 392–399 (2013).
5. Marras, C. et al. Motor and nonmotor heterogeneity of LRRK2-related and idiopathic Parkinson’s disease. Mov. Disord. 31, 1192–1202 (2016).
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