Open AccessExome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction
Author(s) -
Ron Do,
Nathan O. Stitziel,
HongHee Won,
Anders Jørgensen,
Stefano Duga,
Pier Angelica Merlini,
Adam Kieżun,
Martin Farrall,
Anuj Goel,
Or Zuk,
I. Guella,
Rosanna Asselta,
Leslie A. Lange,
Gina M. Peloso,
Paul L. Auer,
Domenico Girelli,
Nicola Martinelli,
Deborah Farlow,
Mark A. DePristo,
Robert Roberts,
Alexander F. R. Stewart,
Danish Saleheen,
John Danesh,
Stephen E. Epstein,
Suthesh Sivapalaratnam,
G. Kees Hovingh,
John J.P. Kastelein,
Nilesh J. Samani,
Heribert Schunkert,
J. Erdmann,
Svati H. Shah,
William E. Kraus
Publication year - 2015
Publication title -
carolina digital repository (university of north carolina at chapel hill)
Language(s) - English
DOI - 10.17615/pc2a-ev84
Subject(s) - exome sequencing , myocardial infarction , allele , exome , genetics , biology , medicine , computational biology , mutation , gene