| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8285452 | Parkinsonism & Related Disorders | 2018 | 29 Pages |
Abstract
In conjunction with long disease duration and aging, our findings suggest that the F52L DCTN1 mutation may evoke severe tauopathy and moderate α-synucleinopathy.
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Authors
Hiroyuki Honda, Naokazu Sasagasako, Chang Shen, Masahiro Shijo, Hideomi Hamasaki, Satoshi O. Suzuki, Yoshio Tsuboi, Naoki Fujii, Toru Iwaki,