N. Vanacore
AuthID: R-00G-1QS
1
TITLE: A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease Full Text
AUTHORS: Di Fonzo, A; Rohe, CF; Ferreira, RJ; Chien, HF; Vacca, L; Stocchi, F; Guedes, L; Fabrizio, E; Manfredi, M; Vanacore, N; Goldwurm, S; Breedveld, G; Sampaio, C; Meco, G; Barbosa, E; Oostra, BA; Bonifati, V;
PUBLISHED: 2005, SOURCE: LANCET, VOLUME: 365, ISSUE: 9457
AUTHORS: Di Fonzo, A; Rohe, CF; Ferreira, RJ; Chien, HF; Vacca, L; Stocchi, F; Guedes, L; Fabrizio, E; Manfredi, M; Vanacore, N; Goldwurm, S; Breedveld, G; Sampaio, C; Meco, G; Barbosa, E; Oostra, BA; Bonifati, V;
PUBLISHED: 2005, SOURCE: LANCET, VOLUME: 365, ISSUE: 9457
