SCN5A mutations and polymorphisms in patients with ventricular fibrillation during acute myocardial infarction

Molecular Medicine Reports

Volumn 10, Issue 4, 2014, Pages 2039-2044

  Boehringer, Tim ^a,b   Bugert, Peter ^a,b   Borggrefe, Martin ^b,c   Elmas, Elif ^b,c  

^a Institute of Transfusion Medicine and Immunology   (Germany)

^b UNIVERSITY OF HEIDELBERG   (Germany)

^c UNIVERSITY OF HEIDELBERG   (Germany)

Author keywords

Arrhythmia; Exon resequencing; Genetic risk factor; Myocardial infarction; SCN5A gene variant; Ventricular fibrillation

Indexed keywords

SODIUM CHANNEL NAV1.5; SCN5A PROTEIN, HUMAN;

ACUTE HEART INFARCTION; ADULT; ALLELE; ARTICLE; BRUGADA SYNDROME; CONTROLLED STUDY; DNA FLANKING REGION; ENTIRE CODING REGION; EXON; FEMALE; GENE; GENE FREQUENCY; GENE STRUCTURE; GENETIC RISK; GENETIC VARIABILITY; GENOTYPE; HEART VENTRICLE FIBRILLATION; HUMAN; INTRON; LONG QT SYNDROME; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; POLYMERASE CHAIN REACTION; PROGRESSIVE CARDIAC CONDUCTION DEFECT; PROMOTER REGION; QT INTERVAL; SINGLE NUCLEOTIDE POLYMORPHISM; SODIUM CHANNEL NAV1.5 GENE; SUDDEN DEATH; SUDDEN INFANT DEATH SYNDROME; WILD TYPE; ACUTE DISEASE; AGED; GENETICS; HEART INFARCTION; MIDDLE AGED; PATHOLOGY; PATIENT;

ACUTE DISEASE; AGED; EXONS; FEMALE; GENE FREQUENCY; GENOTYPE; HUMANS; MALE; MIDDLE AGED; MYOCARDIAL INFARCTION; NAV1.5 VOLTAGE-GATED SODIUM CHANNEL; PATIENTS; POLYMORPHISM, SINGLE NUCLEOTIDE; VENTRICULAR FIBRILLATION;

EID: 84929511528     PISSN: 17912997     EISSN: 17913004     Source Type: Journal    
DOI: 10.3892/mmr.2014.2401     Document Type: Article

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