Cardiac ion channel mutations in the sudden infant death syndrome

International Journal of Cardiology

Volumn 152, Issue 2, 2011, Pages 162-170

  Klaver, Eva C ^a   Versluijs, G Marja ^a   Wilders, Ronald ^a,b  

^a UNIVERSITY OF AMSTERDAM   (Netherlands)

^b NONE   (Netherlands)

Author keywords

Brugada syndrome; Ion channelopathies; Long QT syndrome; Short QT syndrome; Sudden infant death

Indexed keywords

ALPHA1 SYNTROPHIN; CARDIAC ION CHANNEL; CAVEOLIN 3; CONNEXIN 43; GLYCEROL 3 PHOSPHATE DEHYDROGENASE; INWARDLY RECTIFYING POTASSIUM CHANNEL SUBUNIT KIR2.1; INWARDLY RECTIFYING POTASSIUM CHANNEL SUBUNIT KIR6.1; ION CHANNEL; POTASSIUM CHANNEL; POTASSIUM CHANNEL HERG; POTASSIUM CHANNEL KCNE1; POTASSIUM CHANNEL KCNE2; POTASSIUM CHANNEL KCNQ1; RYANODINE RECEPTOR 2; SODIUM CHANNEL; SODIUM CHANNEL NAV1.5; SODIUM CHANNEL SUBUNIT BETA 1; SODIUM CHANNEL SUBUNIT BETA 2; SODIUM CHANNEL SUBUNIT BETA 3; SODIUM CHANNEL SUBUNIT BETA 4; SYNTROPHIN; UNCLASSIFIED DRUG;

AUTONOMIC DYSFUNCTION; CALCIUM CHANNEL GENE; CARDIAC CHANNELOPATHY; CARDIAC ION CHANNEL GENE; GENE; GENE MUTATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC PREDISPOSITION; GENETIC RISK; GENETIC VARIABILITY; HEREDITY; HUMAN; LONG QT SYNDROME; METABOLIC DISORDER; PHENOTYPE; POTASSIUM CHANNEL GENE; PREVALENCE; PRIORITY JOURNAL; PROTEIN POLYMORPHISM; REVIEW; SHORT QT SYNDROME; SODIUM CHANNEL GENE; SUDDEN INFANT DEATH SYNDROME;

EID: 80053576214     PISSN: 01675273     EISSN: 18741754     Source Type: Journal    
DOI: 10.1016/j.ijcard.2010.12.051     Document Type: Review

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