SCN5A Mutation associated with acute myocardial infarction

Legal Medicine

Volumn 11, Issue SUPPL. 1, 2009, Pages

  Oliva, Antonio ^a   Hu, Dan ^b   Viskin, Sami ^c   Carrier, Tabitha ^b   Cordeiro, Jonathan M ^b   Barajas Martinez, Hector ^b   Wu, Yusheng ^b   Burashnikov, Elena ^b   Brugada, Ramon ^b   Rosso, Rafael ^b   Guerchicoff, Alexandra ^b   Pollevick, Guido ^b   Pascali, Vincenzo L ^a   Antzelevitch, Charlie ^b  

^a CATHOLIC UNIVERSITY   (Italy)

^b MASONIC MEDICAL RESEARCH LABORATORY   (United States)

^c TEL AVIV SOURASKY MEDICAL CENTER   (Israel)

Author keywords

Arrhythmia; Fibrillation; Ischemia; Sudden cardiac death; Ventricular tachycardia

Indexed keywords

SODIUM CHANNEL;

ACUTE HEART INFARCTION; ADULT; AGED; ALLELE; ARTICLE; CLINICAL ARTICLE; FEMALE; GENE; GENE EXPRESSION; GENE MUTATION; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENETIC PREDISPOSITION; GENETIC SCREENING; HEART VENTRICLE EXTRASYSTOLE; HEART VENTRICLE FIBRILLATION; HEART VENTRICLE TACHYCARDIA; HETEROZYGOTE; HUMAN; HUMAN CELL; ISCHEMIA; LOSS OF FUNCTION MUTATION; MALE; MISSENSE MUTATION; PATCH CLAMP; SCN1B GENE; SCN5A GENE; SINGLE NUCLEOTIDE POLYMORPHISM; ST SEGMENT; WHOLE CELL; WILD TYPE;

ADULT; AGED; ALLELES; CASE-CONTROL STUDIES; ELECTROCARDIOGRAM PATTERN; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MIDDLE AGED; MUSCLE PROTEINS; MUTATION, MISSENSE; MYOCARDIAL INFARCTION; PATCH-CLAMP TECHNIQUES; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC; SODIUM CHANNELS; TACHYCARDIA, VENTRICULAR; VENTRICULAR FIBRILLATION;

EID: 67349251486     PISSN: 13446223     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.legalmed.2009.02.044     Document Type: Article

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