Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.
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dc.contributor.author | Ghosh, A | |
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dc.contributor.author | Aung, T | |
dc.contributor.author | Ozaki, M | |
dc.contributor.author | Lee, MC | |
dc.contributor.author | Schlötzer-Schrehardt, U | |
dc.contributor.author | Thorleifsson, G | |
dc.contributor.author | Mizoguchi, T | |
dc.contributor.author | Igo, RP | |
dc.contributor.author | Haripriya, A | |
dc.contributor.author | Williams, SE | |
dc.contributor.author | Astakhov, YS | |
dc.contributor.author | Orr, AC | |
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dc.contributor.author | Edward, DP | |
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dc.contributor.author | Moghimi, S | |
dc.contributor.author | Ideta, R | |
dc.contributor.author | Bach-Holm, D | |
dc.contributor.author | Kappelgaard, P | |
dc.contributor.author | Wirostko, B | |
dc.contributor.author | Thomas, S | |
dc.contributor.author | Gaston, D | |
dc.contributor.author | Bedard, K | |
dc.contributor.author | Greer, WL | |
dc.contributor.author | Yang, Z | |
dc.contributor.author | Chen, X | |
dc.contributor.author | Huang, L | |
dc.contributor.author | Sang, J | |
dc.contributor.author | Jia, H | |
dc.contributor.author | Jia, L | |
dc.contributor.author | Qiao, C | |
dc.contributor.author | Zhang, H | |
dc.contributor.author | Liu, X | |
dc.contributor.author | Zhao, B | |
dc.contributor.author | Wang, YX | |
dc.contributor.author | Xu, L | |
dc.contributor.author | Leruez, S | |
dc.contributor.author | Reynier, P | |
dc.contributor.author | Chichua, G | |
dc.contributor.author | Tabagari, S | |
dc.contributor.author | Uebe, S | |
dc.contributor.author | Zenkel, M | |
dc.contributor.author | Berner, D | |
dc.contributor.author | Mossböck, G | |
dc.contributor.author | Weisschuh, N | |
dc.contributor.author | Hoja, U | |
dc.contributor.author | Welge-Luessen, UC | |
dc.contributor.author | Mardin, C | |
dc.contributor.author | Founti, P | |
dc.contributor.author | Chatzikyriakidou, A | |
dc.contributor.author | Pappas, T | |
dc.contributor.author | Anastasopoulos, E | |
dc.contributor.author | Lambropoulos, A | |
dc.date.accessioned | 2021-03-04T18:05:39Z | |
dc.date.available | 2021-03-04T18:05:39Z | |
dc.identifier.citation | Aung T., Ozaki M., Lee M., Schlötzer-Schrehardt U., Thorleifsson G., Mizoguchi T., Igo R., Haripriya A., Williams S., Astakhov Y., et al., "Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.", Nature genetics, cilt.49, ss.993-1004, 2017 | |
dc.identifier.issn | 1061-4036 | |
dc.identifier.other | vv_1032021 | |
dc.identifier.other | av_88e75038-8ea3-4728-921b-433566b192be | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/92872 | |
dc.identifier.uri | https://doi.org/10.1038/ng.3875 | |
dc.language.iso | eng | |
dc.title | Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci. | |
dc.type | Makale | |
dc.relation.journal | Nature genetics | |
dc.contributor.department | , , | |
dc.identifier.volume | 49 | |
dc.identifier.startpage | 993 | |
dc.identifier.endpage | 1004 | |
dc.contributor.firstauthorID | 2208067 |
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