Rare variants in β-Amyloid precursor protein (APP) and Parkinson's disease

Many individuals with Parkinson's disease (PD) develop cognitive deficits, and a phenotypic and molecular overlap between neurodegenerative diseases exists. We investigated the contribution of rare variants in seven genes of known relevance to dementias (β-amyloid precursor protein (APP), PSEN1...

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書誌詳細
出版年:Eur J Hum Genet
主要な著者: Schulte, Eva C, Fukumori, Akio, Mollenhauer, Brit, Hor, Hyun, Arzberger, Thomas, Perneczky, Robert, Kurz, Alexander, Diehl-Schmid, Janine, Hüll, Michael, Lichtner, Peter, Eckstein, Gertrud, Zimprich, Alexander, Haubenberger, Dietrich, Pirker, Walter, Brücke, Thomas, Bereznai, Benjamin, Molnar, Maria J, Lorenzo-Betancor, Oswaldo, Pastor, Pau, Peters, Annette, Gieger, Christian, Estivill, Xavier, Meitinger, Thomas, Kretzschmar, Hans A, Trenkwalder, Claudia, Haass, Christian, Winkelmann, Juliane
フォーマット: Artigo
言語:Inglês
出版事項: Nature Publishing Group 2015
主題:
Article
オンライン･アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4592093/
https://ncbi.nlm.nih.gov/pubmed/25604855
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2014.300
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