Associated Papers
Protein-truncating variants in UQCRC1 are associated with Parkinson's disease: evidence from half-million people.
Jing X et al.
Npj Parkinson's Disease, 2025
UQCRC1 variants in Parkinson's disease: a large cohort study in Chinese mainland population.
Zhao YW et al.
Brain : a Journal of Neurology, 2021
Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy.
Lin CH et al.
Brain : a Journal of Neurology, 2020
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