Chelsea Tu
Vancouver, BC, Canada
Last Updated: 09/26/2026
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Found 9 publications
DCTN1 p.K56R in progressive supranuclear palsy.
Journal: Parkinsonism & related disorders
Published: January 22, 2016
α-synuclein genetic variability: A biomarker for dementia in Parkinson disease.
Journal: Annals of neurology
Published: December 09, 2015
Double homozygous mutations (R275W and M432V) in the ParkinGene associated with late-onset Parkinson's disease.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: August 12, 2015
Novel LRRK2 mutations in Parkinsonism.
Journal: Parkinsonism & related disorders
Published: May 29, 2015
Defining neurodegeneration on Guam by targeted genomic sequencing.
Journal: Annals of neurology
Published: August 14, 2014
Genetic variability of the retromer cargo recognition complex in parkinsonism.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: August 01, 2014
DNAJC13 mutations in Parkinson disease.
Journal: Human molecular genetics
Published: November 13, 2013
STX6 rs1411478 is not associated with increased risk of Parkinson's disease.
Journal: Parkinsonism & related disorders
Published: December 13, 2012
Alpha-synuclein p.H50Q, a novel pathogenic mutation for Parkinson's disease.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: September 11, 2012
Showing 1-9 of 9
Last Updated: 09/26/2026