Disease Progression of GNE Myopathy and Its Relationship With Genotype
Our results provide insights into the motor function involvement observed during disease progression in Chinese patients with GNE myopathy, and relatively mild disease severity was observed in those with the p.D207V mutation.
Authors
- Fuze Zheng
- Jiaxi Yu (ORCID: https://orcid.org/0000-0002-6458-5226)
- Wei Zhang (ORCID: https://orcid.org/0000-0002-5822-9970)
- Lingchao Meng (ORCID: https://orcid.org/0000-0003-3004-6758)
- Haozhe Sun (ORCID: https://orcid.org/0000-0002-3625-2870)
- Meng Yu (ORCID: https://orcid.org/0000-0003-0234-5902)
- He Lv (ORCID: https://orcid.org/0000-0002-4148-625X)
- Yun Yuan (ORCID: https://orcid.org/0000-0003-3282-9123)
- Qiang Gang
- Zhao-xia Wang
Institutions
- Ministry of Education (RO)
Publication Details
- Journal
- Neurology Genetics
- Published
- 2024-11-11
- DOI
- https://doi.org/10.1212/nxg.0000000000200203
- Citations
- 1
- Primary Topic
- Inflammatory Myopathies and Dermatomyositis
- Type
- article
- Field-Weighted Citation Impact
- 0.39
Funders
- Peking University First Hospital
- National Natural Science Foundation of China
- Peking University