Associated Papers
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
R869C mutation in molecular motor KIF17 gene is involved in dementia with Lewy bodies.
Goldstein O et al.
Alzheimer's & Dementia (amsterdam, Netherlands), 2021
34124335 (PubMed )
Supplement: DAD2-13-e12143-s004.pdf
Evaluation of PINK1 variants in Indian Parkinson's disease patients.
Biswas A et al.
Parkinsonism & Related Disorders, 2010
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