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

Victoria E. Jackson (Lead / Corresponding author), Ioanna Ntalla, Ian Sayers, Richard Morris, Peter Whincup, Juan-Pablo Casas, Antoinette Amuzu, Minkyoung Choi, Caroline Dale, Meena Kumari, Jorgen Engmann, Noor Kalsheker, Sally Chappell, Tamar Guetta-Baranes, Tricia M. McKeever, Colin N. A. Palmer, Roger Tavendale, John W. Holloway, Avan A Sayer, Elaine M. DennisonCyrus Cooper, Mona Bafadhel, Bethan Barker, Chris Brightling, Charlotte E. Bolton, Michelle E. John, Stuart G. Parker, Miriam F. Moffat, Andrew J. Wardlaw, Martin J Connolly, David J. Porteous, Blair H. Smith, Sandosh Padmanabhan, Lynne Hocking, Kathleen E. Stirrups, Panos Deloukas, David P. Strachan, Ian P. Hall, Martin D. Tobin, Louise V. Wain

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