Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12. (2016)
Attributed to:
Sarcopenia, Frailty and Clinical Practice in Older People
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1136/thoraxjnl-2015-207876
PubMed Identifier: 26917578
Publication URI: http://europepmc.org/abstract/MED/26917578
Type: Journal Article/Review
Volume: 71
Parent Publication: Thorax
Issue: 6
ISSN: 0040-6376