ATP13A2 variability in Parkinson disease

Recessively inherited mutations in ATP13A2 result in Kufor-Rakeb syndrome, whereas genetic variability and elevated ATP13A2 expression have been implicated in Parkinson disease (PD). Given this background, ATP13A2 was comprehensively assessed to support or refute its contribution to PD. Sequencing o...

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Huvudupphovsmän: Vilariño-Güell, Carles, Soto, Alexandra I., Lincoln, Sarah J., Yahmed, Samia Ben, Kefi, Mounir, Heckman, Michael G., Hulihan, Mary M., Chai, Hua, Diehl, Nancy N., Amouri, Rim, Rajput, Alex, Mash, Deborah C., Dickson, Dennis W., Middleton, Lefkos T., Gibson, Rachel A., Hentati, Faycal, Farrer, Matthew J.
Materialtyp: Artigo
Språk:Inglês
Publicerad: 2009
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Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC2650009/
https://ncbi.nlm.nih.gov/pubmed/19085912
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/humu.20877
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