Article info
Chronic obstructive pulmonary disease
Original article
Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12
- Correspondence to Victoria E Jackson, Department of Health Sciences, University of Leicester, University Road, Leicester LE1 7RH, UK; vej3{at}le.ac.uk
Citation
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
May 13, 2016
Article Versions
- Previous version (25 February 2016).
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Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/