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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:Neurology
मुख्य लेखकों: 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.
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: Lippincott Williams & Wilkins 2014
विषय:
Article
ऑनलाइन पहुंच: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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