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Common variants in Parkinson's disease.
Ross OA, Farrer MJ, Wu RM. Ross OA, et al. Among authors: farrer mj. Mov Disord. 2007 Apr 30;22(6):899-900. doi: 10.1002/mds.21463. Mov Disord. 2007. PMID: 17377919 No abstract available.
Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations.
Kachergus J, Mata IF, Hulihan M, Taylor JP, Lincoln S, Aasly J, Gibson JM, Ross OA, Lynch T, Wiley J, Payami H, Nutt J, Maraganore DM, Czyzewski K, Styczynska M, Wszolek ZK, Farrer MJ, Toft M. Kachergus J, et al. Among authors: farrer mj. Am J Hum Genet. 2005 Apr;76(4):672-80. doi: 10.1086/429256. Epub 2005 Feb 22. Am J Hum Genet. 2005. PMID: 15726496 Free PMC article.
LRRK2 mutations and Parkinsonism.
Toft M, Mata IF, Kachergus JM, Ross OA, Farrer MJ. Toft M, et al. Among authors: farrer mj. Lancet. 2005 Apr 2-8;365(9466):1229-30. doi: 10.1016/S0140-6736(05)74809-1. Lancet. 2005. PMID: 15811454 No abstract available.
451 results