Associated Papers
PRKN/PINK1 Mutations in a Chinese Patient With Early-Onset Parkinson's Disease.
Lu Z et al.
Brain and Behavior, 2025
Rethinking 'rare' PINK1 Parkinson's disease: A meta-analysis of geographical prevalence, phenotypic diversity, and α-synuclein pathology.
Yin EP et al.
Journal of Parkinson's Disease, 2025
39973502 (PubMed )
Supplement: sj-xlsx-2-pkn-10.1177_1877718x241304814.xlsx › Total_PINK1_cases
Association of five SNPs at the PARK16 locus as a susceptibility locus with Parkinson's disease for forensic application.
Cui HG et al.
Fa Yi Xue Za Zhi, 2013
Association of Parkinson's disease with six single nucleotide polymorphisms located in four PARK genes in the northern Han Chinese population.
Zhou Y et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia, 2012
Mutation analysis of parkin and PINK1 genes in early-onset Parkinson's disease in China.
Zhang BR et al.
Neuroscience Letters, 2010
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