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Coronary heart disease and genetic variants with low phospholipase A2 activity.

TitleCoronary heart disease and genetic variants with low phospholipase A2 activity.
Publication TypeJournal Article
Year of Publication2015
AuthorsPolfus LM, Gibbs RA
Secondary AuthorsBoerwinkle E
JournalN Engl J Med
Volume372
Issue3
Pagination295-6
Date Published2015 Jan 15
ISSN1533-4406
KeywordsAfrican Americans, Aged, Coronary Disease, European Continental Ancestry Group, Exome, Female, Genetic Variation, Heterozygote, Humans, Male, Middle Aged, Mutation, Phospholipases A2, Risk Factors
DOI10.1056/NEJMc1409673
Alternate JournalN Engl J Med
PubMed ID25587968
PubMed Central IDPMC4339029
Grant ListHHSN268201100012C / HL / NHLBI NIH HHS / United States
RC2 HL102419 / HL / NHLBI NIH HHS / United States
HHSN268201100009I / HL / NHLBI NIH HHS / United States
HHSN268201100010C / HL / NHLBI NIH HHS / United States
HHSN268201100008C / HL / NHLBI NIH HHS / United States
HHSN268201100005G / HL / NHLBI NIH HHS / United States
HHSN268201100008I / HL / NHLBI NIH HHS / United States
HHSN268201100005C / / PHS HHS / United States
HHSN268201100007C / HL / NHLBI NIH HHS / United States
HHSN268201100009C / / PHS HHS / United States
HHSN268201100011I / HL / NHLBI NIH HHS / United States
HHSN268201100011C / HL / NHLBI NIH HHS / United States
U54 HG003273 / HG / NHGRI NIH HHS / United States
HHSN268201100010C / / PHS HHS / United States
HHSN268201100006C / HL / NHLBI NIH HHS / United States
HHSN268201100008C / / PHS HHS / United States
HHSN268201100012C / / PHS HHS / United States
HHSN268201100005I / HL / NHLBI NIH HHS / United States
RC2HL102419 / HL / NHLBI NIH HHS / United States
HHSN268201100007C / / PHS HHS / United States
HHSN268201100009C / HL / NHLBI NIH HHS / United States
HHSN268201100011C / / PHS HHS / United States
HHSN268201100005C / HL / NHLBI NIH HHS / United States
HHSN268201100007I / HL / NHLBI NIH HHS / United States
HHSN268201100006C / / PHS HHS / United States