Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing

Heart Rhythm

Volumn 2, Issue 5, 2005, Pages 507-517

  Tester, David J ^a   Will, Melissa L ^a   Haglund, Carla M ^a   Ackerman, Michael J ^a,b  

^a Mayo Clinic   (United States)

^b MAYO CLINIC   (United States)

Author keywords

Genetic testing; Long QT syndrome; Potassium channels; Sodium channels

Indexed keywords

ION CHANNEL; POTASSIUM CHANNEL; POTASSIUM CHANNEL KCNQ1;

ADOLESCENT; ADULT; AGED; ARTICLE; CHILD; CONTROLLED STUDY; DNA SEQUENCE; EXON; FEMALE; GENE MUTATION; GENETIC CODE; GENETIC SCREENING; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; INFANT; LABORATORY TEST; LONG QT SYNDROME; MAJOR CLINICAL STUDY; MALE; MEMBRANE CHANNEL; MISSENSE MUTATION; OPEN READING FRAME; PATIENT REFERRAL; POLYMERASE CHAIN REACTION; POTASSIUM CHANNEL KCNE1; POTASSIUM CHANNEL KCNE2; POTASSIUM CHANNEL KCNH; POTASSIUM CHANNEL SCN5A; PRIORITY JOURNAL; PUBLICATION; RNA SPLICING;

ADOLESCENT; ADULT; AGED; CHILD; CHILD, PRESCHOOL; DNA MUTATIONAL ANALYSIS; FEMALE; GENOTYPE; HUMANS; INFANT; INFANT, NEWBORN; KCNQ POTASSIUM CHANNELS; KCNQ1 POTASSIUM CHANNEL; LONG QT SYNDROME; MALE; MIDDLE AGED; MUTATION; PHENOTYPE; POTASSIUM CHANNELS, VOLTAGE-GATED; SODIUM CHANNELS;

EID: 17144415220     PISSN: 15475271     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.hrthm.2005.01.020     Document Type: Article

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