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Publications by Joanne Trinh

LRP10 in Α-Synucleinopathies

The Lancet Neurology
Neurology
2018English

De Novo Variants in TAOK1 Cause Neurodevelopmental Disorders

American Journal of Human Genetics
Genetics
2019English

MtDNA Deletions Discriminate Affected From Unaffected LRRK2 Mutation Carriers

Annals of Neurology
Neurology
2019English

Mild Dopa-Responsive Dystonia in Heterozygous Tyrosine Hydroxylase Mutation Carrier: Evidence of Symptomatic Enzyme Deficiency?

Parkinsonism and Related Disorders
GerontologyGeriatricsNeurology
2020English

The Role of Rare Coding Variants in Parkinson's Disease GWAS Loci

Frontiers in Neurology
Neurology
2019English

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