✦ LIBER ✦

Screening for SNCA and LRRK2 mutations in Greek sporadic and autosomal dominant Parkinson's disease: identification of two novel LRRK2 variants

✍ Scribed by G. Xiromerisiou; G. M. Hadjigeorgiou; V. Gourbali; J. Johnson; I. Papakonstantinou; A. Papadimitriou; A. B. Singleton

Book ID: 111064866
Publisher: John Wiley and Sons
Year: 2007
Tongue: English
Weight: 491 KB
Volume: 14
Category: Article
ISSN: 1351-5101
DOI: 10.1111/j.1468-1331.2006.01551.x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Screening for LRRK2 mutations in patient

Screening for LRRK2 mutations in patients with Parkinson’s disease in Russia: identification of a novel LRRK2 variant

✍ S. N. Pchelina; A. F. Yakimovskii; A. K. Emelyanov; O. N. Ivanova; A. L. Schwarz 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 164 KB

High prevalence of LRRK2 mutations in fa

High prevalence of LRRK2 mutations in familial and sporadic Parkinson's disease in Portugal

✍ Joaquim J. Ferreira; Leonor Correia Guedes; Mário Miguel Rosa; Miguel Coelho; Ma 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 122 KB 👁 1 views

## Abstract Mutations in the __Leucine‐Rich Repeat Kinase 2__ (__LRRK2__) gene are the most frequent known cause of Parkinson's disease (PD), but their prevalence varies markedly between populations. Here we studied the frequency and associated phenotype of four recurrent __LRRK2__ mutations (R1441

Comprehensive LRRK2 and GBA screening in

Comprehensive LRRK2 and GBA screening in Portuguese patients with Parkinson's disease: Identification of a new family with the LRRK2 p.Arg1441His mutation and novel missense variants

✍ Zhang, Lei; Quadri, Marialuisa; Guedes, Leonor Correia; Coelho, Miguel; Valadas, 📂 Article 📅 2013 🏛 Elsevier Science 🌐 English ⚖ 267 KB

3.026 MUTATIONAL ANALYSIS OF PARK2, SNCA

3.026 MUTATIONAL ANALYSIS OF PARK2, SNCA AND LRRK2 IN PARKINSON'S DISEASE PATIENTS OF SOUTH INDIA

✍ P. Vishwanathan; A.V. Srinivasan; M. Jayaraman; C.R.S. Srisailapathy; A. Ramesh 📂 Article 📅 2012 🏛 Elsevier Science 🌐 English ⚖ 56 KB

Analysis of Parkinson disease patients f

Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2

✍ Jose Bras; Rita Guerreiro; Maria Ribeiro; Ana Morgadinho; Cristina Januario; Mar 📂 Article 📅 2008 🏛 BioMed Central 🌐 English ⚖ 964 KB

Type and frequency of mutations in the L

Type and frequency of mutations in the LRRK2 gene in familiar and sporadic Parkinson's disease

✍ Berg, D. 📂 Article 📅 2005 🏛 Oxford University Press 🌐 English ⚖ 271 KB