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Identification of a rare coding variant in complement 3 associated with age-related macular degeneration

dc.contributor.authorZhan, X
dc.contributor.authorLarson, DE
dc.contributor.authorWang, C
dc.contributor.authorKoboldt, DC
dc.contributor.authorSergeev, YV
dc.contributor.authorFulton, RS
dc.contributor.authorFulton, LL
dc.contributor.authorFronick, CC
dc.contributor.authorBranham, KE
dc.contributor.authorBragg-Gresham, J
dc.contributor.authorJun, G
dc.contributor.authorHu, Y
dc.contributor.authorKang, HM
dc.contributor.authorLiu, D
dc.contributor.authorOthman, M
dc.contributor.authorBrooks, M
dc.contributor.authorRatnapriya, R
dc.contributor.authorBoleda, A
dc.contributor.authorGrassmann, F
dc.contributor.authorvon Strachwitz, C
dc.contributor.authorOlson, LM
dc.contributor.authorBuitendijk, GHS
dc.contributor.authorHofman, A
dc.contributor.authorvan Duijn, CM
dc.contributor.authorCipriani, V
dc.contributor.authorMoore, AT
dc.contributor.authorShahid, H
dc.contributor.authorJiang, Y
dc.contributor.authorConley, YP
dc.contributor.authorMorgan, DJ
dc.contributor.authorKim, IK
dc.contributor.authorJohnson, MP
dc.contributor.authorCantsilieris, S
dc.contributor.authorRichardson, AJ
dc.contributor.authorGuymer, RH
dc.contributor.authorLuo, H
dc.contributor.authorOuyang, H
dc.contributor.authorLicht, C
dc.contributor.authorPluthero, FG
dc.contributor.authorZhang, MM
dc.contributor.authorZhang, K
dc.contributor.authorBaird, PN
dc.contributor.authorBlangero, J
dc.contributor.authorKlein, ML
dc.contributor.authorFarrer, LA
dc.contributor.authorDeAngelis, MM
dc.contributor.authorWeeks, DE
dc.contributor.authorGorin, MB
dc.contributor.authorYates, JRW
dc.contributor.authorKlaver, CCW
dc.contributor.authorPericak-Vance, MA
dc.contributor.authorHaines, JL
dc.contributor.authorWeber, BHF
dc.contributor.authorWilson, RK
dc.contributor.authorHeckenlively, JR
dc.contributor.authorChew, EY
dc.contributor.authorStambolian, D
dc.contributor.authorMardis, ER
dc.contributor.authorSwaroop, A
dc.contributor.authorAbecasis, GR
dc.date.accessioned2021-01-20T17:26:52Z
dc.date.available2013-08-19
dc.date.available2021-01-20T17:26:52Z
dc.date.issued2013-09-15
dc.identifier.citationZhan, X., Larson, D., Wang, C. et al. Identification of a rare coding variant in complement 3 associated with age-related macular degeneration. Nat Genet 45, 1375–1379 (2013). https://doi.org/10.1038/ng.2758en_US
dc.identifier.issn1061-4036
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/69887
dc.format.extent1375–1379
dc.relation.ispartofNATURE GENETICS
dc.titleIdentification of a rare coding variant in complement 3 associated with age-related macular degenerationen_US
dc.typeArticleen_US
dc.identifier.doi10.1038/ng.2758
pubs.author-urlhttp://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000326384100020&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=612ae0d773dcbdba3046f6df545e9f6aen_US
pubs.issue11en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume45en_US
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US
qmul.funderCentre for Health service and Academic Partnership in Translational eHealth Research (CHAPTER)::Medical Research Councilen_US


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