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