Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease

OBJECTIVE: Leucine-rich repeat kinase 2 (LRRK2) mutations are the most common cause of Parkinson disease (PD). Several dominantly inherited pathogenic substitutions have been identified in different domains of the Lrrk2 protein. Herein, we characterize the clinical and genetic features associated wi...

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Detaylı Bibliyografya
Asıl Yazarlar: Haugarvoll, K., Rademakers, R., Kachergus, J.M., Nuytemans, K., Ross, O.A., Gibson, J.M., Tan, E.-K., Gaig, C., Tolosa, E., Goldwurm, S., Guidi, M., Riboldazzi, G., Brown, L., Walter, U., Benecke, R., Berg, D., Gasser, T., Theuns, J., Pals, P., Cras, P., De Deyn, P. Paul, Engelborghs, S., Pickut, B., Uitti, R.J., Foroud, T., Nichols, W.C., Hagenah, J., Klein, C., Samii, A., Zabetian, C.P., Bonifati, V., Van Broeckhoven, C., Farrer, M.J., Wszolek, Z.K.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2008
Konular:
Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3906630/
https://ncbi.nlm.nih.gov/pubmed/18337586
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/01.wnl.0000304044.22253.03
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