No large-effect low-frequency coding variation found for myocardial infarction

Human Molecular Genetics

Volumn 23, Issue 17, 2014, Pages 4721-4728

  Holmen, Oddgeir L ^a,b   Zhang, He ^c   Zhou, Wei ^c   Schmidt, Ellen ^c   Hovelson, Daniel H ^c   Langhammer, Arnulf ^a   Løchen, Maja Lisa ^d   Ganesh, Santhi K ^c   Mathiesen, Ellisiv B ^d,e   Vatten, Lars ^a   Platou, Carl ^a   Wilsgaard, Tom ^d   Chen, Jin ^c   Skorpen, Frank ^a   Dalen, Håvard ^a,f   Boehnke, Michael ^g   Abecasis, Goncalo R ^g   Njølstad, Inger ^d   Hveem, Kristian ^a,f   Willer, Cristen J ^c  

^a NORWEGIAN UNIVERSITY OF SCIENCE AND TECHNOLOGY   (Norway)

^b TRONDHEIM UNIVERSITY HOSPITAL   (Norway)

^c UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

^d UNIVERSITY OF TROMSØ   (Norway)

^e UNIVERSITY HOSPITAL OF NORTH NORWAY   (Norway)

^f Levanger Hospital   (Norway)

^g UNIVERSITY OF MICHIGAN SCHOOL OF PUBLIC HEALTH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ALLELE; ARTICLE; CODING; CORONARY ARTERY DISEASE; EFFECT SIZE; EXOME; FEMALE; GENE FREQUENCY; GENE SEQUENCE; GENETIC VARIABILITY; GENOTYPE; HEART INFARCTION; HUMAN; MAJOR CLINICAL STUDY; MALE; NORWAY; PRIORITY JOURNAL; GENETIC PREDISPOSITION; GENETICS; HUMAN GENOME; OPEN READING FRAME; RISK FACTOR; SINGLE NUCLEOTIDE POLYMORPHISM;

EXOME; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENETIC VARIATION; GENOME, HUMAN; HUMANS; MALE; MYOCARDIAL INFARCTION; OPEN READING FRAMES; POLYMORPHISM, SINGLE NUCLEOTIDE; RISK FACTORS;

EID: 84905641946     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddu175     Document Type: Article

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