A Homoplasmic <i>MT‐TV</i> Mutation Associated with Mitochondrial Inheritance of Hereditary Spastic Paraplegia
The rare MT-TV m.1661A > G mutation is associated with HSP. Variations in mtDNA copy number may play a causal role in differences among clinical phenotypes. © 2024 International Parkinson and Movement Disorder Society.
Authors
- Junyi Jiang (ORCID: https://orcid.org/0000-0002-4080-069X)
- Shunyan Hong (ORCID: https://orcid.org/0000-0002-9174-5299)
- Wan‐Jin Chen (ORCID: https://orcid.org/0000-0002-9472-8494)
- Xuejiao Chen (ORCID: https://orcid.org/0000-0002-0697-9534)
- Jiyuan Liu
- Xiang Lin (ORCID: https://orcid.org/0000-0002-1449-0114)
- Ning Wang (ORCID: https://orcid.org/0000-0002-2663-7515)
- Junhao Xie (ORCID: https://orcid.org/0009-0003-0805-0424)
- Xinyu Yan (ORCID: https://orcid.org/0000-0001-7558-0626)
- Guorong Xu
- Hui‐Zhen Su
- Yan Shi
Institutions
- Fujian Medical University (CN)
- Zhangzhou Municipal Hospital of Fujian Province (CN)
- First Affiliated Hospital of Fujian Medical University (CN)
Publication Details
- Journal
- Movement Disorders
- Published
- 2024-10-28
- DOI
- https://doi.org/10.1002/mds.30048
- Primary Topic
- Hereditary Neurological Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China
- Natural Science Foundation of Fujian Province
- Fujian Provincial Health Technology Project