LRRK2 G2019S as a Cause of Parkinson's Disease in North African Arabs
✍ Scribed by Lesage, Suzanne; Dürr, Alexandra; Tazir, Meriem; Lohmann, Ebba; Leutenegger, Anne-Louise; Janin, Sabine; Pollak, Pierre; Brice, Alexis
- Book ID
- 124079846
- Publisher
- Massachusetts Medical Society
- Year
- 2006
- Tongue
- English
- Weight
- 136 KB
- Volume
- 354
- Category
- Article
- ISSN
- 0096-6762
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Posterior cortical atrophy (PCA) represents a degenerative disorder characterized by the development of higherorder visual deficit. 1 PCA may result from heterogeneous pathologies that make up tauopathies. An increasing number of mutations in the tau gene (microtubule-associated protein tau [MAPT])
## Abstract Among mutations associated with autosomal dominant and sporadic Parkinson's disease (PD) the G2019S substitution in the leucine‐rich repeat kinase 2 (LRRK2) gene is the most frequently identified. To estimate its frequency in Russia, we analyzed 208 patients with PD from the Northwester