A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease

作者：Alessio Di Fonzo, Christan F. Rohé, Joaquim José Ferreira, Hsin Fen Chien, Laura Vacca, Fabrizio Stocchi, Leonor Correia Guedes, Edito Fabrizio, Mario Manfredi, Nicola Vanacore, Stefano Goldwurm, Guido J. Breedveld, Cristina Matos Sampaio, Giuseppe Meco, Egberto Reis Barbosa, Ben A. Oostra, Vincenzo Bonifati · 发表于：The Lancet · 年份：2005 · DOI：10.1016/s0140-6736(05)17829-5 · 被引用次数：538 · 研究领域：Parkinson's Disease Mechanisms and Treatments、Neurological diseases and metabolism、Nuclear Receptors and Signaling