Rare Genetic Variants in PARN Are Associated with Pulmonary Fibrosis in Families
Am J Respir Crit Care Med
.
2017 Dec 1;196(11):1481-1484.
doi: 10.1164/rccm.201703-0635LE.
Authors
Jonathan A Kropski
1
,
Sara Reiss
1
,
Cheryl Markin
1
,
Kevin K Brown
2
,
David A Schwartz
2
3
,
Marvin I Schwarz
3
,
James E Loyd
1
,
John A Phillips 3rd
1
,
Timothy S Blackwell
1
4
,
Joy D Cogan
1
Affiliations
1
1 Vanderbilt University Medical Center Nashville, Tennessee.
2
2 National Jewish Health Denver, Colorado.
3
3 University of Colorado Denver, School of Medicine Denver, Colorado and.
4
4 Department of Veterans Affairs Medical Center Nashville, Tennessee.
PMID:
28414520
PMCID:
PMC5736978
DOI:
10.1164/rccm.201703-0635LE
No abstract available
Publication types
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, Non-P.H.S.
MeSH terms
Genetic Variation / genetics*
Humans
Pulmonary Fibrosis / genetics*
Grants and funding
P01 HL092870/HL/NHLBI NIH HHS/United States
K08 HL130595/HL/NHLBI NIH HHS/United States
U54 HL127672/HL/NHLBI NIH HHS/United States
T32 HL094296/HL/NHLBI NIH HHS/United States
R01 HL085317/HL/NHLBI NIH HHS/United States
UM1 HG006493/HG/NHGRI NIH HHS/United States
R01 HL097163/HL/NHLBI NIH HHS/United States
UL1 RR024975/RR/NCRR NIH HHS/United States
R33 HL120770/HL/NHLBI NIH HHS/United States