MAPT haplotype diversity in multiple system atrophy

INTRODUCTION: Multiple system atrophy (MSA) is a rare progressive neurodegenerative disorder. MSA was originally considered exclusively sporadic but reports of association with genes such as SNCA, COQ2 and LRRK2 have demonstrated that there is a genetic contribution to the disease. MAPT has been ass...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Parkinsonism Relat Disord
Asıl Yazarlar: Labbé, Catherine, Heckman, Michael G., Lorenzo-Betancor, Oswaldo, Murray, Melissa E., Ogaki, Kotaro, Soto-Ortolaza, Alexandra I., Walton, Ronald L., Fujioka, Shinsuke, Koga, Shunsuke, Uitti, Ryan J., van Gerpen, Jay A., Petersen, Ronald C., Graff-Radford, Neill R., Younkin, Steven G., Boeve, Bradley F., Cheshire, William P., Low, Phillip A., Sandroni, Paola, Coon, Elizabeth A., Singer, Wolfgang, Wszolek, Zbigniew K., Dickson, Dennis W., Ross, Owen A.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2016
Konular:
Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5007155/
https://ncbi.nlm.nih.gov/pubmed/27374978
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.parkreldis.2016.06.010
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!

Benzer Materyaller