𝔖 Bobbio Scriptorium
✦   LIBER   ✦

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


Kin-cohort analysis of LRRK2-G2019S pene
✍ Stefano Goldwurm; Sara Tunesi; Silvana Tesei; Michela Zini; Francesca Sironi; Pa 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 1023 KB

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])

G2019S LRRK2 mutation in familial and sp
✍ Sofya N. Pchelina; Andrei F. Yakimovskii; Olga N. Ivanova; Anton K. Emelianov; A 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 80 KB

## 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