The role of ATP13A2 in Parkinson's disease: Clinical phenotypes and molecular mechanisms
Author:
Affiliation:
1. Department of Neurogenetics; Kolling Institute of Medical Research, Royal North Shore Hospital and the University of Sydney; St. Leonards New South Wales Australia
Funder
Brain Foundation and the Parkinson's New South Wales Association
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/mds.26243/fullpdf
Reference65 articles.
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3. Kufor-Rakeb syndrome, pallido-pyramidal degeneration with supranuclear upgaze paresis and dementia, maps to 1p36;Hampshire;J Med Genet,2001
4. Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase;Ramirez;Nat Genet,2006
5. a-Synuclein is part of a diverse and highly conserved interaction network that includes PARK9 and manganese toxicity;Gitler;Nat Genet,2009
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