<i>PRKN/PINK1</i> Mutations in a Chinese Patient With Early‐Onset Parkinson's Disease
PRKN/PINK1 mutations may be linked to compromised mitophagy pathways. Genetic screening is significant for EOPD patients, especially those with specific symptoms and ethnic backgrounds.
Authors
- Mei Xin (ORCID: https://orcid.org/0000-0002-5732-7501)
- Rongyang Dai (ORCID: https://orcid.org/0000-0002-7126-1713)
- Yunlan Du
- Gang Chen (ORCID: https://orcid.org/0000-0001-8112-3579)
- Ye Sun
- Zhongjiao Lu (ORCID: https://orcid.org/0000-0003-3347-4352)
- Hualong Wang (ORCID: https://orcid.org/0000-0002-5741-0313)
- Liemei Guo
- Gang Wang (ORCID: https://orcid.org/0000-0003-0252-488X)
Institutions
- Shanghai Jiao Tong University (CN)
- Renji Hospital (CN)
Publication Details
- Journal
- Brain and Behavior
- Published
- 2025-09-01
- DOI
- https://doi.org/10.1002/brb3.70822
- Citations
- 3
- Primary Topic
- Parkinson's Disease Mechanisms and Treatments
- Type
- article
- Field-Weighted Citation Impact
- 4.17
Funders
- National Natural Science Foundation of China