Testing association between LRRK2 and Parkinson's disease and investigating linkage disequilibrium

BACKGROUND: We and others recently identified the gene underlying PARK8 linked Parkinson's disease (PD). This gene, LRRK2, contains mutations that cause an autosomal dominant PD, including a mutation, G2019S, which is the most common PD causing mutation identified to date. Common genetic variab...

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書誌詳細
主要な著者: Paisán‐Ruíz, C, Evans, E W, Jain, S, Xiromerisiou, G, Gibbs, J R, Eerola, J, Gourbali, V, Hellström, O, Duckworth, J, Papadimitriou, A, Tienari, P J, Hadjigeorgiou, G M, Singleton, A B
フォーマット: Artigo
言語:Inglês
出版事項: BMJ Group 2006
主題:
Electronic Letter
オンライン･アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC2564648/
https://ncbi.nlm.nih.gov/pubmed/16467219
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2005.036889
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