Genetic and Clinical Features of Progranulin-Associated Frontotemporal Lobar Degeneration

OBJECTIVE: To assess the relative frequency of unique mutations and their associated characteristics in 97 individuals with mutations in progranulin (GRN), an important cause of frontotemporal lobar degeneration (FTLD). PARTICIPANTS AND DESIGN: A 46-site International Frontotemporal Lobar Degenerati...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: Chen-Plotkin, Alice S., Martinez-Lage, Maria, Sleiman, Patrick M. A., Hu, William, Greene, Robert, Wood, Elisabeth McCarty, Bing, Shaoxu, Grossman, Murray, Schellenberg, Gerard D., Hatanpaa, Kimmo J., Weiner, Myron F., White, Charles L., Brooks, William S., Halliday, Glenda M., Kril, Jillian J., Gearing, Marla, Beach, Thomas G., Graff-Radford, Neill R., Dickson, Dennis W., Rademakers, Rosa, Boeve, Bradley F., Pickering-Brown, Stuart M., Snowden, Julie, van Swieten, John C., Heutink, Peter, Seelaar, Harro, Murrell, Jill R., Ghetti, Bernardino, Spina, Salvatore, Grafman, Jordan, Kaye, Jeffrey A., Woltjer, Randall L., Mesulam, Marsel, Bigio, Eileen, Lladó, Albert, Miller, Bruce L., Alzualde, Ainhoa, Moreno, Fermin, Rohrer, Jonathan D., Mackenzie, Ian R. A., Feldman, Howard H., Hamilton, Ronald L., Cruts, Marc, Engelborghs, Sebastiaan, De Deyn, Peter P., Van Broeckhoven, Christine, Bird, Thomas D., Cairns, Nigel J., Goate, Allison, Frosch, Matthew P., Riederer, Peter F., Bogdanovic, Nenad, Lee, Virginia M. Y., Trojanowski, John Q., Van Deerlin, Vivianna M.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2011
Konular:
Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3160280/
https://ncbi.nlm.nih.gov/pubmed/21482928
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/archneurol.2011.53
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!

Benzer Materyaller