Lack of evidence for association of UQCRC1 with autosomal dominant Parkinson's disease in Caucasian families

Author:

Courtin Thomas,Tesson Christelle,Corvol Jean-Christophe,Lesage Suzanne,Brice Alexis,

Funder

Association France Parkinson

Prix Allianz

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Genetics (clinical),Genetics

Reference5 articles.

1. Lin C-H, Tsai P-I, Lin H-Y, Hattori N, Funayama M, Jeon B, Sato K, Abe K, Mukai Y, Takahashi Y, Li Y, Nishioka K, Yoshino H, Daida K, Chen M-L, Cheng J, Huang C-Y, Tzeng S-R, Wu Y-S, Lai H-J, Tsai H-H, Yen R-F, Lee N-C, Lo W-C, Hung Y-C, Chan C-C, Ke Y-C, Chao C-C, Hsieh S-T, Farrer M, Wu R-M (2020) Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy. Brain 143:3352–3373. https://doi.org/10.1093/brain/awaa279

2. Senkevich K, Bandres-Ciga S, Gan-Or Z, Krohn L, International Parkinson’s Disease Genomics Consortium (IPDGC) (2020) Lack of evidence for association of UQCRC1 with Parkinson’s disease in Europeans. Neurobiol Aging. https://doi.org/10.1016/j.neurobiolaging.2020.10.030

3. Lin Z-H, Zheng R, Ruan Y, Gao T, Jin C-Y, Xue N-J, Dong J-X, Yan Y-P, Tian J, Pu J-L, Zhang B-R (2020) The lack of association between ubiquinol-cytochrome c reductase core protein I (UQCRC1) variants and Parkinson’s disease in an eastern Chinese population. CNS Neurosci Ther 26:990–992. https://doi.org/10.1111/cns.13436

4. Zhao Y-W, Pan H-X, Wang C-Y, Zeng Q, Wang Y, Fang Z-H, Huang J, Li X, Wang X, Zhang X, Liu Z-H, Sun Q-Y, Xu Q, Lei L-F, Yan X-X, Shen L, Jiang H, Tan J-Q, Li J-C, Tang B-S, Zhang H-N, Guo J-F (2021) UQCRC1 variants in Parkinson’s disease: a large cohort study in Chinese mainland population. Brain. https://doi.org/10.1093/brain/awab137

5. Vital A, Lepreux S, Vital C (2014) Peripheral neuropathy and parkinsonism: a large clinical and pathogenic spectrum. J Peripher Nerv Syst 19:333–342. https://doi.org/10.1111/jns.12099

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