UQCRC1 variants in Parkinson’s disease: a large cohort study in Chinese mainland population-Reference-Cited by-同舟云学术

UQCRC1 variants in Parkinson’s disease: a large cohort study in Chinese mainland population

Published:2021-03-29 Issue:6 Volume:144 Page:e54-e54
ISSN:0006-8950
Container-title:Brain
language:en
Short-container-title:

Author:

Zhao Yu-wen¹²,Pan Hong-xu¹²,Wang Chun-yu³,Zeng Qian¹,Wang Yige¹,Fang Zheng-huan⁴,Huang Juanjuan¹,Li Xiaosong⁵,Wang Xiaoye⁶,Zhang Xi⁷,Liu Zhen-hua¹,Sun Qi-ying⁸,Xu Qian¹,Lei Li-fang⁹,Yan Xin-xiang¹,Shen Lu¹²¹⁰,Jiang Hong¹²¹⁰^ORCID,Tan Jie-qiong⁴,Li Jin-chen²⁴⁸^ORCID,Tang Bei-sha¹²⁴¹⁰^ORCID,Zhang Hai-nan³,Guo Ji-feng¹²⁴¹⁰^ORCID

Affiliation:

1. Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China

2. National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China

3. Department of Neurology, The Second Xiangya Hospital, Central South University, Changsha, Hunan 410011, China

4. Centre for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan 410008, China

5. Hunan Provincial People’s Hospital, The First Affiliated Hospital of Hunan Normal University, Changsha, Hunan 410007, China

6. Department of General Surgery, Brain Hospital of Hunan province, Changsha, Hunan 410007, China

7. Department of Neurology, Brain Hospital of Hunan province, Changsha, Hunan 410007, China

8. Department of Geriatrics, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China

9. Department of Neurology, The Third Xiangya Hospital, Central South University, Changsha, Hunan 410013, China

10. Key Laboratory of Hunan Province in Neurodegenerative Disorders, Central South University, Changsha, Hunan 410008, China

Funder

National Key Research and Development Program of China

Central Public-Interest Scientific Institution Basal Research Fund of Chinese Academy of Medical Sciences

National Natural Science Foundation of China

Science and Technology Major Project of Hunan Provincial Science and Technology Department

Department of Science & Technology of Hunan Province

Innovation-driven Team Project from Central South University

Publisher

Oxford University Press (OUP)

Subject

Clinical Neurology

Link

http://academic.oup.com/brain/advance-article-pdf/doi/10.1093/brain/awab137/38377688/awab137.pdf

Reference10 articles.

1. Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy;Lin;Brain,2020

2. A clinical and genetic study of early-onset and familial parkinsonism in taiwan: An integrated approach combining gene dosage analysis and next-generation sequencing;Lin;Mov Disord,2019

3. Rare genetic variation in mitochondrial pathways influences the risk for Parkinson's disease;Gaare;Mov Disord,2018

4. The role of genetics in Parkinson's disease: A large cohort study in Chinese mainland population;Zhao;Brain,2020

5. GCH1 variants contribute to the risk and earlier age-at-onset of Parkinson's disease: A two-cohort case-control study;Pan;Transl Neurodegener,2020

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1. Rare variant analysis of UQCRC1 in Chinese patients with early-onset Parkinson’s disease;Neurobiology of Aging;2024-02

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3. UQCRC1 variants in early-onset and familial Parkinson's disease in a Taiwanese cohort;Frontiers in Neurology;2022-12-09

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