Novel Variants in <scp> <i>DCTN1</i> </scp> Associated with Perry Disease: A Case Series from a Chinese Parkinsonism Cohort
Our study broadens the genetic and phenotypic spectrum of Perry disease. These findings support consideration of DCTN1 CAP-Gly domain-related variants in patients with parkinsonism to facilitate early recognition and management. © 2026 International Parkinson and Movement Disorder Society.
Authors
- Xiaosheng Zheng (ORCID: https://orcid.org/0000-0002-2710-6775)
- Nan Jin (ORCID: https://orcid.org/0000-0002-3263-1144)
- Yiling Elaine Chen (ORCID: https://orcid.org/0000-0001-7259-2787)
- Bo Wang (ORCID: https://orcid.org/0000-0001-9234-035X)
- Chenxin Ying
- Wei Luo (ORCID: https://orcid.org/0000-0002-3821-7796)
- J. Li
- Zhidong Cen
- Yixin Kang
- Yiying Zhang
- Xinhui Chen
- Yaoting Wang
Institutions
- Second Affiliated Hospital of Zhejiang University (CN)
Publication Details
- Journal
- Movement Disorders
- Published
- 2026-02-22
- DOI
- https://doi.org/10.1002/mds.70244
- Primary Topic
- Skin and Cellular Biology Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00