Serveur d'exploration sur la maladie de Parkinson

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The G2019S LRRK2 mutation is uncommon amongst Greek patients with sporadic Parkinson's disease

Identifieur interne : 000F41 ( Main/Exploration ); précédent : 000F40; suivant : 000F42

The G2019S LRRK2 mutation is uncommon amongst Greek patients with sporadic Parkinson's disease

Auteurs : K. Kalinderi [Grèce] ; L. Fidani [Grèce] ; S. Bostantjopoulou [Grèce] ; Z. Katsarou [Grèce] ; A. Kotsis [Grèce]

Source :

RBID : ISTEX:0E35C463024562ADDCC87D7F105411C10D63BE6A

English descriptors

Abstract

Parkinson's disease (PD) is the second most common neurodegenerative disorder affecting approximately 2% of the population >60 years of age. Although, the etiology of PD is still unknown, the genetic background of the disease has been documented. Recently, a mutation in the LRRK2 gene, G2019S, was associated with 3–41% and 1–2% of familial and sporadic PD, respectively suggesting a pivotal role of LRRK2 in PD. In this report, we examine the association of the G2019S mutation with sporadic late‐onset PD, in an independent cohort of Greek patients and controls.

Url:
DOI: 10.1111/j.1468-1331.2007.01867.x


Affiliations:


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