Biallelic expansion in RFC1 as a rare cause of Parkinson's disease.

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第一作者： Laura,Kytövuori

第一单位： Research Unit of Clinical Neuroscience, Medical Research Center Oulu, Oulu University Hospital and University of Oulu, Oulu, Finland. laura.kytovuori@oulu.fi.

作者： Laura,Kytövuori ^[1] ; Jussi,Sipilä ^[2] ; Hiroshi,Doi ^[3] ; Anri,Hurme-Niiranen ^[4] ; Ari,Siitonen ^[5] ; Eriko,Koshimizu ^[6] ; Satoko,Miyatake ^[7] ; Naomichi,Matsumoto ^[6] ; Fumiaki,Tanaka ^[7] ; Kari,Majamaa ^[8]

作者单位： Research Unit of Clinical Neuroscience, Medical Research Center Oulu, Oulu University Hospital and University of Oulu, Oulu, Finland. laura.kytovuori@oulu.fi. ^[1] Department of Neurology, Oulu University Hospital, Oulu, Finland. laura.kytovuori@oulu.fi. ^[2] Clinical Neurosciences, University of Turku, Turku, Finland. ^[3] Department of Neurology, Siun Sote North Karelia Central Hospital, Joensuu, Finland. ^[4] Department of Neurology and Stroke Medicine, Yokohama City University Graduate School of Medicine, Yokohama, Japan. ^[5] Research Unit of Clinical Neuroscience, Medical Research Center Oulu, Oulu University Hospital and University of Oulu, Oulu, Finland. ^[6] Department of Neurology, Oulu University Hospital, Oulu, Finland. ^[7] Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan. ^[8] Clinical Genetics Department, Yokohama City University Hospital, Yokohama, Japan. ^[9]

DOI 10.1038/s41531-021-00275-7

PMID 35013364

发布时间 2022-01-21

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NPJ Parkinson's disease

2022年8卷1期

6页

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Biallelic expansion in RFC1 as a rare cause of Parkinson's disease.

NPJ Parkinson's disease

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NPJ Parkinson's disease

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Biallelic expansion in RFC1 as a rare cause of Parkinson's disease.

NPJ Parkinson's disease

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NPJ Parkinson's disease

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