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...

詳細記述

保存先:
書誌詳細
出版年:Parkinsonism Relat Disord
主要な著者: 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.
フォーマット: Artigo
言語:Inglês
出版事項: 2016
主題:
Article
オンライン･アクセス: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
タグ: タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!

類似資料