Genome-wide association study of maternal and inherited loci for conotruncal heart defects

PLoS ONE

Volumn 9, Issue 5, 2014, Pages

  Agopian, A J ^a   Mitchell, Laura E ^a   Glessner, Joseph ^c   Bhalla, Angela D ^a   Sewda, Anshuman ^a   Hakonarson, Hakon ^b,c   Goldmuntz, Elizabeth ^b,c  

^a UNIVERSITY OF TEXAS SCHOOL OF PUBLIC HEALTH   (United States)

^b UNIVERSITY OF PENNSYLVANIA   (United States)

^c CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CARDIOVASCULAR RISK; CHROMOSOME 11Q; CHROMOSOME 22Q; CONGENITAL HEART MALFORMATION; CONOTRUNCAL HEART DEFECT; DISEASE ASSOCIATION; FEMALE; GENE; GENE LOCUS; GENETIC ASSOCIATION; GENETIC IDENTIFICATION; GENETIC RISK; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GENOTYPE; HUMAN; INHERITANCE; INTRON; KCNJ4 GENE; MAJOR CLINICAL STUDY; MALE; MOTHER; RISK ASSESSMENT; SINGLE NUCLEOTIDE POLYMORPHISM; SLC22A24 GENE; GENETICS;

INWARDLY RECTIFYING POTASSIUM CHANNEL; KCNJ4 PROTEIN, HUMAN;

FEMALE; GENETIC LOCI; GENOME-WIDE ASSOCIATION STUDY; HEART DEFECTS, CONGENITAL; HUMANS; MALE; POLYMORPHISM, SINGLE NUCLEOTIDE; POTASSIUM CHANNELS, INWARDLY RECTIFYING;

EID: 84900400677     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0096057     Document Type: Article

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