LRRK2 exonic variants and risk of multiple system atrophy

OBJECTIVE: The aim of this study was to evaluate the association between common exonic variants in the leucine-rich repeat kinase 2 (LRRK2) gene and risk of multiple system atrophy (MSA). METHODS: One series from the United States (92 patients with pathologically confirmed MSA, 416 controls) and a s...

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Publicado no:Neurology
Main Authors: Heckman, Michael G., Schottlaender, Lucia, Soto-Ortolaza, Alexandra I., Diehl, Nancy N., Rayaprolu, Sruti, Ogaki, Kotaro, Fujioka, Shinsuke, Murray, Melissa E., Cheshire, William P., Uitti, Ryan J., Wszolek, Zbigniew K., Farrer, Matthew J., Sailer, Anna, Singleton, Andrew B., Chinnery, Patrick F., Keogh, Michael J., Gentleman, Steve M., Holton, Janice L., Aoife, Kiely, Mann, David M.A., Al-Sarraj, Safa, Troakes, Claire, Dickson, Dennis W., Houlden, Henry, Ross, Owen A.
Formato: Artigo
Idioma:Inglês
Publicado em: Lippincott Williams & Wilkins 2014
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4277668/
https://ncbi.nlm.nih.gov/pubmed/25378673
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0000000000001078
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