Human Genome Epidemiology Literature Finder
|
Records 1 - 2 (of 2 Records) |
| Query Trace: Aphasia and LRRK2[original query] |
|---|
| Corticobasal syndrome and primary progressive aphasia as manifestations of LRRK2 gene mutations. Neurology 2008 Feb 70 (7): 521-7. Chen-Plotkin A S, Yuan W, Anderson C, McCarty Wood E, Hurtig H I, Clark C M, Miller B L, Lee V M-Y, Trojanowski J Q, Grossman M, Van Deerlin V |
| Genetic Screening of Patients with Sporadic Alzheimer's Disease and Frontotemporal Lobar Degeneration in the Chinese Population. Journal of Alzheimer's disease : JAD 2024 5 . Yaoru Li, Ziying Yang, Yanxin Zhang, Fang Liu, Jing Xu, Yaping Meng, Gebeili Xing, Xuqin Ruan, Jun Sun, Nan Zha |
- Page last reviewed:Feb 1, 2024
- Content source:

