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

Jackson, V E, Ntalla, I, Sayers, I, Morris, R, Whincup, P, Casas, J-P, Amuzu, A, Choi, M, Dale, C, Kumari, M, Engmann, J, Kalsheker, N, Chappell, S, Guetta-Baranes, T, McKeever, T M, Palmer, C N A, Tavendale, R, Holloway, J W, Sayer, A A, Dennison, E M, Cooper, C, Bafadhel, M, Barker, B, Brightling, C, Bolton, C E, John, M E, Parker, S G, Moffat, M F, Wardlaw, A J, Connolly, M J, Porteous, D J, Smith, B H, Padmanabhan, S, Hocking, L, Stirrups, K E, Deloukas, P, Strachan, D P, Hall, I P, Tobin, M D & Wain, L V 2016, 'Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12', Thorax, vol. 71, no. 6, pp. 501-509. https://doi.org/10.1136/thoraxjnl-2015-207876