Associated Papers
Exome sequencing in Asian populations identifies low-frequency and rare coding variation influencing Parkinson's disease risk.
Chew EG et al.
Nature Aging, 2025
39572736 (PubMed )
Supplement: 43587_2024_760_MOESM3_ESM.xlsx › Supplementary_Table_12
Mutation analysis of LRP10 in a large Chinese familial Parkinson disease cohort.
Li C et al.
Neurobiology of Aging, 2021
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