Rare variant analysis of UQCRC1 in Chinese patients with early-onset Parkinson’s disease-Reference-Cited by-同舟云学术

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Rare variant analysis of UQCRC1 in Chinese patients with early-onset Parkinson’s disease

Published:2024-02 Issue: Volume:134 Page:40-42
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Wang Shichan,Zheng Xiaoting,Ou Ruwei,Wei Qianqian,Lin Junyu,Yang Tianmi,Xiao Yi,Jiang Qirui,Li Chunyu,Shang Huifang^ORCID

Funder

West China Hospital, Sichuan University

Sichuan Province Science and Technology Support Program

National Key Research and Development Program of China

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Neurology (clinical),Aging,General Neuroscience

Reference11 articles.

1. Large-scale pathway specific polygenic risk and transcriptomic community network analysis identifies novel functional pathways in Parkinson disease;Bandres-Ciga;Acta Neuropathol.,2020

2. The ChinaMAP analytics of deep whole genome sequences in 10,588 individuals;Cao;Cell Res.,2020

3. The mutation spectrum of Parkinson-disease-related genes in early-onset Parkinson's disease in ethnic Chinese;Chen;Eur. J. Neurol.,2022

4. Lack of evidence for association of UQCRC1 with autosomal dominant Parkinson's disease in Caucasian families;Courtin;Neurogenetics,2021

5. Complete coding sequence, intron/exon organization, and chromosomal location of the gene for the core I protein of human ubiquinol-cytochrome c reductase;Hoffman;J. Biol. Chem.,1993

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