학술논문

Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
Document Type
Artikel
Author
van Rheenen, Wvan der Spek, RAABakker, MKvan Vugt, JJFAHop, PJZwamborn, RAJde Klein, NWestra, HJBakker, OBDeelen, PShireby, GHannon, EMoisse, MBaird, DRestuadi, RDolzhenko, EDekker, AMGawor, KWesteneng, HJTazelaar, GHPvan Eijk, KRKooyman, MByrne, RPDoherty, MHeverin, MAl Khleifat, AIacoangeli, AShatunov, ATicozzi, NCooper-Knock, JSmith, BNGromicho, MChandran, SPal, SMorrison, KEShaw, PJHardy, JOrrell, RWSendtner, MMeyer, TBasak, Nvan der Kooi, AJRatti, AFogh, IGellera, CLauria, GCorti, SCereda, CSproviero, DD'Alfonso, SSoraru, GSiciliano, GFilosto, MPadovani, AChio, ACalvo, AMoglia, CBrunetti, MCanosa, AGrassano, MBeghi, EPupillo, ELogroscino, GNefussy, BOsmanovic, ANordin, ALerner, YZabari, MGotkine, MBaloh, RHBell, SVourc'h, PCorcia, PCouratier, PMillecamps, SMeininger, VSalachas, FPardina, JMSAssialioui, ARojas-Garcia, RDion, PARoss, JPLudolph, ACWeishaupt, JHBrenner, DFreischmidt, ABensimon, GBrice, ADurr, APayan, CAMSaker-Delye, SWood, NWTopp, SRademakers, RTittmann, LLieb, WFranke, ARipke, SBraun, AKraft, JWhiteman, DCOlsen, CMUitterlinden, AGHofman, ARietschel, MCichon, SNothen, MMAmouyel, PComi, GRiva, NLunetta, CGerardi, FCotelli, MSRinaldi, FChiveri, LGuaita, MCPerrone, PCeroni, MDiamanti, LFerrarese, CTremolizzo, LDelodovici, MLBono, GManera, UVasta, RBombaci, ACasale, FFuda, GSalamone, PIazzolino, BPeotta, LCugnasco, PDe Marco, GTorrieri, MCPalumbo, FGallone, SBarberis, MSbaiz, LGentile, SMauro, AMazzini, LDe Marchi, FCorrado, LBertolotto, AGionco, MLeotta, DOdddenino, EImperiale, DCavallo, RPignatta, PDe Mattei, MGeda, CPapurello, DMGusmaroli, GComi, CLabate, CRuiz, LFerrandi, DRota, EAguggia, MDi Vito, NMeineri, PGhiglione, PLaunaro, NDotta, MDi Sapio, AGiardini, GTiloca, CPeverelli, STaroni, FPensato, VCastellotti, BComi, GPDel Bo, RGagliardi, SRaggi, FSimoncini, CLo Gerfo, AInghilleri, MFerlini, ASimone, ILPassarella, BGuerra, VZoccolella, SNozzoli, CMundi, CLeone, MZarrelli, MTamma, FValluzzi, FCalabrese, GBoero, GRini, ATraynor, BJSingleton, ABNeto, MMCauchi, RJOphoff, RAWiedau-Pazos, MLomen-Hoerth, Cvan Deerlin, VMGrosskreutz, JRoediger, AGaur, NJork, ABarthel, TTheele, EIlse, BStubendorff, BWitte, OWSteinbach, RHubner, CAGraff, CBrylev, LFominykh, VDemeshonok, VAtaulina, ARogelj, BKoritnik, BZidar, JRavnik-Glavac, MGlavac, DStevic, ZDrory, VPovedano, MBlair, IPKiernan, MCBenyamin, BHenderson, RDFurlong, SMathers, SMcCombe, PANeedham, MNgo, STNicholson, GAPamphlett, RRowe, DBSteyn, FJWilliams, KLMather, KASachdev, PSHenders, AKWallace, Lde Carvalho, MPinto, SPetri, SWeber, MRouleau, GASilani, VCurtis, CJBreen, GGlass, JDBrown, RHLanders, JEShaw, CEAndersen, PMGroen, EJNvan Es, MAPasterkamp, RJFan, DSGarton, FCMcRae, AFSmith, GDGaunt, TREberle, MAMill, JMcLaughlin, RLHardiman, OKenna, KPWray, NRTsai, ELRunz, HFranke, LAl-Chalabi, AVan Damme, Pvan den Berg, LHVeldink, JH
Source
Nature genetics. 54(3):361-361
Subject
Medicin och hälsovetenskap
Language
English
English
ISSN
1546-1718