Associated Papers
Rare and novel variants of PRKN and PINK1 genes in Vietnamese patients with early-onset Parkinson's disease.
Ton ND et al.
Molecular Genetics & Genomic Medicine, 2020
Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update.
Nuytemans K et al.
Human Mutation, 2010
20506312 (PubMed )
Supplement: humu0031-0763-SD1.pdf
Genotype-phenotype correlates in Taiwanese patients with early-onset recessive Parkinsonism.
Lee MJ et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2009
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