| Literature DB >> 20721916 |
Javier Ruiz-Martínez1, Ana Gorostidi, Berta Ibañez, Ainhoa Alzualde, David Otaegui, Fermin Moreno, Adolfo López de Munain, Alberto Bergareche, Juan Carlos Gómez-Esteban, José F Martí Massó.
Abstract
The LRRK2 R1441G mutation was first identified in Basque families and it is responsible for 46% of familial Parkinson's disease (PD) and for 2.5% of sporadic PD in the PD population of Basque ascent. The aim of this study was to determine LRRK2 R1441G penetrance in PD in the Basque Country (Spain) to help in a more accurate genetic counseling. A total of 59 sibships containing 244 individuals, with a total of 40 PD-affected relatives, were studied. Genetic testing for the R1441G mutation in the LRRK2 gene was performed in 133 individuals and was positive in 51% of them. Lifetime penetrance of R1441G mutations turned out to be 12.5% at 65 years to 83.4% at 80 years. No gender differences were found in penetrance.Entities:
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Year: 2010 PMID: 20721916 DOI: 10.1002/mds.23278
Source DB: PubMed Journal: Mov Disord ISSN: 0885-3185 Impact factor: 10.338