A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease.
Di Fonzo A; Rohé CF; Ferreira J; 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; Lancet, 2005, vol. 365, issue 9457, p 412, ISSN 1474547x. ISBN 1474547x.

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