Title | Coronary heart disease and genetic variants with low phospholipase A2 activity. |
Publication Type | Journal Article |
Year of Publication | 2015 |
Authors | Polfus, LM, Gibbs, RA, Boerwinkle, E |
Journal | N Engl J Med |
Volume | 372 |
Issue | 3 |
Pagination | 295-6 |
Date Published | 2015 Jan 15 |
ISSN | 1533-4406 |
Keywords | African Americans, Aged, Coronary Disease, European Continental Ancestry Group, Exome, Female, Genetic Variation, Heterozygote, Humans, Male, Middle Aged, Mutation, Phospholipases A2, Risk Factors |
DOI | 10.1056/NEJMc1409673 |
Alternate Journal | N. Engl. J. Med. |
PubMed ID | 25587968 |
PubMed Central ID | PMC4339029 |
Grant List | HHSN268201100005C / HL / NHLBI NIH HHS / United States HHSN268201100005C / / PHS HHS / United States HHSN268201100006C / HL / NHLBI NIH HHS / United States HHSN268201100006C / / PHS HHS / United States HHSN268201100007C / HL / NHLBI NIH HHS / United States HHSN268201100007C / / PHS HHS / United States HHSN268201100008C / HL / NHLBI NIH HHS / United States HHSN268201100008C / / PHS HHS / United States HHSN268201100009C / HL / NHLBI NIH HHS / United States HHSN268201100009C / / PHS HHS / United States HHSN268201100010C / HL / NHLBI NIH HHS / United States HHSN268201100010C / / PHS HHS / United States HHSN268201100011C / HL / NHLBI NIH HHS / United States HHSN268201100011C / / PHS HHS / United States HHSN268201100012C / / PHS HHS / United States RC2 HL102419 / HL / NHLBI NIH HHS / United States RC2HL102419 / HL / NHLBI NIH HHS / United States U54 HG003273 / HG / NHGRI NIH HHS / United States U54 HG003273 / HG / NHGRI NIH HHS / United States |