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Parkinsonism & Related Disorders|June 24, 2006
The SCA17 phenotype can include features of MSA-C, PSP and cognitive impairmentI-Sheng Lin, Ruey-Meei Wu, Guey-Jen Lee-Chen, et al.
Neuropsychiatric Disease and Treatment|March 21, 2009
Whole genome association studies of neuropsychiatric disease: An emerging era of collaborative genetic discoveryMargaret A Keller, Katrina Gwinn, Josefina Nash, et al.
Neuroscience Letters|April 18, 2002
The tau H1 haplotype is associated with Parkinson's disease in the Norwegian populationMatt Farrer, Lisa Skipper, Marianne Berg, et al.
Genetic Testing|December 20, 2002
Accurate determination of ataxin-2 polyglutamine expansion in patients with intermediate-range repeatsJennifer Hussey, Paul J Lockhart, William Seltzer, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 16, 2004
A consanguineous Turkish family with early-onset Parkinson's disease and an exon 4 parkin deletionOkan Dogu, Janel Johnson, Dena Hernandez, et al.
Archives of Neurology|January 12, 2005
Parkin mutations and early-onset parkinsonism in a Taiwanese cohortRuey-Meei Wu, Rebecca Bounds, Sarah Lincoln, et al.
Neuroscience Letters|January 25, 2005
Unaltered alpha-synuclein blood levels in juvenile Parkinsonism with a parkin exon 4 deletionDavid W Miller, Anthony Crawley, Katrina Gwinn-Hardy, et al.
Plos One|October 27, 2010
CoAIMs: a cost-effective panel of ancestry informative markers for determining continental originsEric R Londin, Margaret A Keller, Cathleen Maista, et al.
Brain : a Journal of Neurology|January 23, 2004
Association between cardiac denervation and parkinsonism caused by alpha-synuclein gene triplicationAmanda Singleton, Katrina Gwinn-Hardy, Yehonotan Sharabi, et al.
Parkinsonism & Related Disorders|July 11, 2003
Mutation at the SCA17 locus is not a common cause of parkinsonismDena Hernandez, Melissa Hanson, Amanda Singleton, et al.
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