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Volumn 71, Issue 6, 2016, Pages 501-509

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

(40)  Jackson, Victoria E a   Ntalla, Ioanna a,b   Sayers, Ian c   Morris, Richard d,e   Whincup, Peter f   Casas, Juan Pablo e,g   Amuzu, Antoinette h   Choi, Minkyoung h   Dale, Caroline h   Kumari, Meena e,i   Engmann, Jorgen e   Kalsheker, Noor c   Chappell, Sally c   Guetta Baranes, Tamar c   McKeever, Tricia M c   Palmer, Colin N A j   Tavendale, Roger j   Holloway, John W k,l   Sayer, Avan A m,n   Dennison, Elaine M m,o   more..


Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; AIRWAY OBSTRUCTION; ANCESTRY GROUP; ARTICLE; CHRNA5 GENE; CHRONIC OBSTRUCTIVE LUNG DISEASE; CLINICAL ASSESSMENT TOOL; CONTROLLED STUDY; DISEASE SEVERITY; EUROPEAN; EXOME; FEMALE; FOLLOW UP; FORCED EXPIRATORY VOLUME; FUNCTIONAL ASSESSMENT; GENE; GENETIC ASSOCIATION; GENETIC CODE; GENETIC RISK; GENETIC VARIABILITY; GENOME ANALYSIS; GENOTYPE; GPR126 GENE; HHIP GENE; HUMAN; IFIT3 GENE; LUNG FUNCTION TEST; MAJOR CLINICAL STUDY; MALE; META ANALYSIS (TOPIC); MMP12 GENE; MOCS3 GENE; POPULATION BASED CASE CONTROL STUDY; POPULATION RESEARCH; PREDICTION; PRIORITY JOURNAL; RISK ASSESSMENT; SERPINA12 GENE; SINGLE NUCLEOTIDE POLYMORPHISM; SMOKING; EPIDEMIOLOGY; GENETICS; GENOME-WIDE ASSOCIATION STUDY; MIDDLE AGED; PATHOPHYSIOLOGY;

EID: 84959273257     PISSN: 00406376     EISSN: 14683296     Source Type: Journal    
DOI: 10.1136/thoraxjnl-2015-207876     Document Type: Article
Times cited : (22)

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