LRRK2exonic variants and risk of multiple system atrophy

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.
Source :: Neurology (Ovid); December 2014, Vol. 83 Issue: 24 p2256-2261, 6p
Publication Year :: 2014
Abstract: 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).

Full Text Access

Tools