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...

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Библиографические подробности
Опубликовано в: :Parkinsonism Relat Disord
Главные авторы: 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.
Формат: Artigo
Язык:Inglês
Опубликовано: 2016
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Article
Online-ссылка: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
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