Author(s): Brás, JM ; Guerreiro, RJ ; Ribeiro, MH ; Januário, C ; Morgadinho, A ; Oliveira, CR ; Hardy, J ; Singleton, A
Date: 2005
Persistent ID: http://hdl.handle.net/10400.4/464
Origin: Repositório do Centro Hospitalar e Universitário de Coimbra
Subject(s): Predisposição Genética para Doença; Doença de Parkinson; Mutação
LRRK2 mutations have recently been described in families with Parkinson's disease. Here we show that one of them (G2019S) is present in 6% (7 of 124) unrelated cases of disease in a clinic-based sample series from central Portugal, but not present in 126 controls from the same population. Thus, LRRK2 mutations appear to be a common cause of typical Parkinson's disease and as such will alter clinical practice.
