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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Pubblicato in:Neurology
Autori principali: 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.
Natura: Artigo
Lingua:Inglês
Pubblicazione: Lippincott Williams & Wilkins 2014
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Article
Accesso online: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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