Novel KCNJ2 mutation associated with Andersen-Tawil syndrome;Nova mutacija kanalčka KCNJ2 pri bolnicis sindromom Andersen-Tawil

Zdravniski Vestnik

Volumn 82, Issue 1, 2013, Pages 55-60

  Šinkovec, Matjaž ^a   Pernat, Andrej ^a   Jan, Matevž ^a   Antolič, Bor ^a   Kovač, Jernej ^a   Podkrajs̀ek, Katarina Trebus̀ak ^a   Debeljak, Maruša ^a  

^a UNIVERSITY MEDICAL CENTRE LJUBLJANA   (Slovenia)

Author keywords

Andersen Tawil syndrome; Bidirectional ventricular tachycardia; Catheter ablation; Genetic disorder; KCNJ2 mutation

Indexed keywords

AMIODARONE; BISOPROLOL; CHLORIDE ION; DILTIAZEM; INWARDLY RECTIFYING POTASSIUM CHANNEL SUBUNIT KIR2.1; POTASSIUM; PROPAFENONE; SOTALOL; VERAPAMIL;

ADULT; ANDERSEN SYNDROME; ARTICLE; CASE REPORT; CATHETER ABLATION; DEFIBRILLATION; DRUG WITHDRAWAL; ELECTROCARDIOGRAPHY; ELECTROLYTE DISTURBANCE; FEMALE; GENETIC ASSOCIATION; GENETIC SCREENING; HEART PALPITATION; HEART VENTRICLE ARRHYTHMIA; HUMAN; HYPERTELORISM; IMPLANTED HEART PACEMAKER; KCNJ2 GENE; MUTATIONAL ANALYSIS; NUCLEOTIDE SEQUENCE; PHYSICAL EXAMINATION; POTASSIUM BLOOD LEVEL; QT PROLONGATION; THORAX PAIN; THYROTOXICOSIS;

EID: 84874219646     PISSN: 13180347     EISSN: 15810224     Source Type: Journal    
DOI: None     Document Type: Article

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