CALM3 mutation associated with long QT syndrome

Heart Rhythm

Volumn 12, Issue 2, 2015, Pages 419-422

  Reed, Griffin J ^a   Boczek, Nicole J ^a,b,c   Etheridge, Susan P ^d   Ackerman, Michael J ^a,c,e  

^a MAYO GRADUATE SCHOOL   (United States)

^b Society for Clinical and Translational Science   (United States)

^c MAYO CLINIC   (United States)

^d PRIMARY CHILDREN'S MEDICAL CENTER   (United States)

^e Cardiovascular Diseases   (United States)

Author keywords

Arrhythmia; Calcium channelinactivation; CALM3; Calmodulin; Genetics; Long QTsyndrome

Indexed keywords

APGAR SCORE; ARTICLE; ATRIOVENTRICULAR BLOCK; BRADYCARDIA; CALM3 GENE; CARDIOMEGALY; CASE REPORT; ELECTROCARDIOGRAM; FAMILY HISTORY; FETUS ECHOGRAPHY; GENE; GENE MUTATION; GENETIC ASSOCIATION; HEART RATE; HUMAN; INFANT; LONG QT SYNDROME; MALE; MEDICAL HISTORY; PRIORITY JOURNAL; QT INTERVAL; SINUS RHYTHM; THORAX RADIOGRAPHY; ADULT; ELECTROCARDIOGRAPHY; GENETICS; METABOLISM; MUTATION; NUCLEOTIDE SEQUENCE; PATHOPHYSIOLOGY; PEDIGREE;

CLATHRIN ASSEMBLY PROTEIN; DNA; PICALM PROTEIN, HUMAN;

ADULT; DNA; DNA MUTATIONAL ANALYSIS; ELECTROCARDIOGRAPHY; HUMANS; LONG QT SYNDROME; MALE; MONOMERIC CLATHRIN ASSEMBLY PROTEINS; MUTATION; PEDIGREE;

EID: 84921064860     PISSN: 15475271     EISSN: 15563871     Source Type: Journal    
DOI: 10.1016/j.hrthm.2014.10.035     Document Type: Article

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