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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Publicado no:Parkinsonism Relat Disord
Main Authors: 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.
Formato: Artigo
Idioma:Inglês
Publicado em: 2016
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Article
Acesso em linha: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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