Associated Papers
The pharmacogenomic landscape in the Chinese: An analytics of pharmacogenetic variants in 206,640 individuals.
Wang LY et al.
Innovation (cambridge (mass.)), 2025
39991480 (PubMed )
Supplement: mmc5.xlsx › Sheet1
UQCRC1 variants in early-onset and familial Parkinson's disease in a Taiwanese cohort.
Liao TW et al.
Frontiers in Neurology, 2022
Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy.
Lin CH et al.
Brain : a Journal of Neurology, 2020
33141179 (PubMed )
Supplement: awaa279_supplementary_data.zip › awaa279-suppl_data › brain-2020-00357-File010.pdf
Select a paper to view details