Coinheritance of long QT syndrome and Kearns-Sayre syndrome

Heart Rhythm

Volumn 4, Issue 12, 2007, Pages 1568-1572

  Skinner, Jonathan R ^a   Yang, Tao ^b   Purvis, Dianne ^a   Chung, Seo Kyung ^a,c   Roden, Dan M ^b   Rees, Mark I ^a,c  

^a STARSHIP CHILDREN S HOSPITAL   (New Zealand)

^b VANDERBILT UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c Wessex Clinical Genetics Service   (United Kingdom)

Author keywords

Complete atrioventricular block; Kearns Sayre syndrome; Long QT syndrome mutation; Mitochondrial disorder; Torsades de pointes

Indexed keywords

LACTIC ACID; MITOCHONDRIAL DNA; NADOLOL; POTASSIUM; POTASSIUM CHANNEL KCNQ1;

ADOLESCENT; ARTICLE; ARTIFICIAL HEART PACEMAKER; ATRIOVENTRICULAR BLOCK; CASE REPORT; ELECTROCARDIOGRAM; FAILURE TO THRIVE; FEMALE; FOLLOW UP; GENE DELETION; GENE MUTATION; HEART RIGHT BUNDLE BRANCH BLOCK; HOSPITAL ADMISSION; HUMAN; HUMAN TISSUE; HYPOKALEMIA; INHERITANCE; KEARNS SAYRE SYNDROME; LACTATE BLOOD LEVEL; LONG QT SYNDROME; METABOLIC ACIDOSIS; MUSCLE BIOPSY; OPHTHALMOPLEGIA; PERCEPTION DEAFNESS; PHENOTYPE; PRIORITY JOURNAL; PTOSIS; QT INTERVAL; RESUSCITATION; RETINA PIGMENT DEGENERATION; SYNCOPE; TORSADE DES POINTES; TUBULAR DYSFUNCTION;

ADOLESCENT; AMINO ACID SEQUENCE; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; KCNQ1 POTASSIUM CHANNEL; KEARNS-SAYER SYNDROME; LONG QT SYNDROME; MOLECULAR SEQUENCE DATA; MUTATION; PHENOTYPE;

EID: 36749011258     PISSN: 15475271     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.hrthm.2007.08.013     Document Type: Article

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