Genetic risk factors for cognitive decline in Parkinson's disease: a review of the literature
Author:
Affiliation:
1. Institute of Clinical Medicine; University of Oslo; Oslo Norway
2. Department of Neurology; Oslo University Hospital; Oslo Norway
Funder
Norwegian Health Association
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/ene.13258/fullpdf
Reference88 articles.
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2. Comparison of kindreds with parkinsonism and alpha-synuclein genomic multiplications;Farrer;Ann Neurol,2004
3. Genetic variability in SNCA and Parkinson's disease;Pihlstrom;Neurogenetics,2011
4. Systematic review and UK-based study of PARK2 (parkin), PINK1, PARK7 (DJ-1) and LRRK2 in early-onset Parkinson's disease;Kilarski;Mov Disord,2012
5. Worldwide frequency of G2019S LRRK2 mutation in Parkinson's disease: a systematic review;Correia Guedes;Parkinsonism Relat Disord,2010
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