A novel KCNQ1 splicing mutation in patients with forme fruste LQT1 aggravated by hypokalemia

Journal of Cardiology

Volumn 64, Issue 2, 2014, Pages 121-126

  Imai, Michiko ^a   Nakajima, Tadashi ^b   Kaneko, Yoshiaki ^b   Niwamae, Nogiku ^a   Irie, Tadanobu ^b   Ota, Masaki ^b   Iijima, Takafumi ^b   Tange, Shoichi ^a   Kurabayashi, Masahiko ^b  

^a MAEBASHI RED CROSS HOSPITAL   (Japan)

^b GUNMA UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

Author keywords

Genetics; Potassium; QT syndrome inherited; Ventricular arrhythmia

Indexed keywords

POTASSIUM; POTASSIUM CHANNEL; POTASSIUM CHANNEL KCNE1; POTASSIUM CHANNEL KCNE2; POTASSIUM CHANNEL KCNH2; POTASSIUM CHANNEL KCNQ1; SODIUM CHANNEL NAV1.5; UNCLASSIFIED DRUG; KCNQ1 PROTEIN, HUMAN;

ADOLESCENT; ADULT; ARTICLE; CARDIOPULMONARY ARREST; CLINICAL ARTICLE; CONTROLLED STUDY; EXON; FAINTNESS; FEMALE; GENE MUTATION; GENETIC ANALYSIS; HEART VENTRICLE TACHYCARDIA; HETEROZYGOTE; HUMAN; HYPOKALEMIA; LONG QT SYNDROME 1; MALE; POTASSIUM BLOOD LEVEL; QT INTERVAL; QT PROLONGATION; RESUSCITATION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; YOUNG ADULT; COMPLICATION; GENETICS; MUTATION; PHENOTYPE; ROMANO-WARD SYNDROME; TACHYCARDIA, VENTRICULAR;

ADOLESCENT; ADULT; EXONS; FEMALE; HUMANS; HYPOKALEMIA; KCNQ1 POTASSIUM CHANNEL; MALE; MUTATION; PHENOTYPE; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; ROMANO-WARD SYNDROME; TACHYCARDIA, VENTRICULAR; YOUNG ADULT;

EID: 84905575197     PISSN: 09145087     EISSN: 18764738     Source Type: Journal    
DOI: 10.1016/j.jjcc.2013.11.014     Document Type: Article

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