Genetic variation of Omi/HtrA2 and Parkinson’s disease

Variants in the Omi/HtrA2 gene have been nominated as a cause of Parkinson’s disease. This sequencing study of Omi/HtrA2 in 95 probands with apparent autosomal dominant inheritance of Parkinson’s disease did not identify any pathogenic mutations. In addition, there was no association between common...

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Detaylı Bibliyografya
Asıl Yazarlar: Ross, Owen A., Soto, Alexandra I., Vilariño-Güell, Carles, Heckman, Michael G., Diehl, Nancy N., Hulihan, Mary M., Aasly, Jan O., Sando, Sigrid, Mark Gibson, J., Lynch, Timothy, Krygowska-Wajs, Anna, Opala, Grzegorz, Barcikowska, Maria, Czyzewski, Krzysztof, Uitti, Ryan J., Wszolek, Zbigniew K., Farrer, Matthew J.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2008
Konular:
Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2614082/
https://ncbi.nlm.nih.gov/pubmed/18790661
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.parkreldis.2008.08.003
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