LRRK2<sup>G2019S</sup> Gene Mutation Causes Skeletal Muscle Impairment in Animal Model of Parkinson's Disease
Taken together, these findings may provide new insights into the clinical and pathogenic involvement of LRRK2<sup>G2019</sup> mutation in muscles, suggesting that the diseases may affect not only midbrain dopaminergic neurons, but also other tissues, and it may help overall clinical management of this devastating disease.
Authors
- Weidong Le (ORCID: https://orcid.org/0000-0001-7459-2705)
- Chunli Song (ORCID: https://orcid.org/0000-0001-5028-5567)
- Tianbai Li (ORCID: https://orcid.org/0000-0002-8554-6373)
- Murad Al‐Nusaif (ORCID: https://orcid.org/0000-0001-7009-7555)
- Lulu Tian (ORCID: https://orcid.org/0000-0001-5820-0337)
- Yiying Hu
- Cheng Cheng (ORCID: https://orcid.org/0000-0002-6179-4882)
- Panpan Wang (ORCID: https://orcid.org/0000-0003-4009-1456)
- Song Li (ORCID: https://orcid.org/0000-0003-2713-9136)
- Zhanhua Liang (ORCID: https://orcid.org/0000-0001-6483-4758)
- Huijia Yang
Institutions
- Dalian Medical University (CN)
- First Affiliated Hospital of Dalian Medical University (CN)
Publication Details
- Journal
- Journal of Cachexia Sarcopenia and Muscle
- Published
- 2024-09-23
- DOI
- https://doi.org/10.1002/jcsm.13604
- Citations
- 4
- Primary Topic
- Muscle Physiology and Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.94
Funders
- National Natural Science Foundation of China