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

Authors

  1. Correspondence to Victoria E Jackson, Department of Health Sciences, University of Leicester, University Road, Leicester LE1 7RH, UK; vej3{at}le.ac.uk
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Citation

Jackson VE, Ntalla I, Sayers I, et al
Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12

Publication history

  • Received September 24, 2015
  • Revised January 5, 2016
  • Accepted January 29, 2016
  • First published February 25, 2016.
Online issue publication 
September 01, 2022

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