Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12.

Jackson, VE; Ntalla, I; Sayers, I; Morris, R; Whincup, P; Casas, JP; Amuzu, A; Choi, M; Dale, C; Kumari, M; +30 more... Engmann, J; Kalsheker, N; Chappell, S; Guetta-Baranes, T; McKeever, TM; Palmer, CN; Tavendale, R; Holloway, JW; Sayer, AA; Dennison, EM; Cooper, C; Bafadhel, M; Barker, B; Brightling, C; Bolton, CE; John, ME; Parker, SG; Moffat, MF; Wardlaw, AJ; Connolly, MJ; Porteous, DJ; Smith, BH; Padmanabhan, S; Hocking, L; Stirrups, KE; Deloukas, P; Strachan, DP; Hall, IP; Tobin, MD; Wain, LV; (2016) Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12. Thorax, 71 (6). pp. 501-9. ISSN 0040-6376 DOI: https://doi.org/10.1136/thoraxjnl-2015-207876

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