From gene to disease; Ion channel proteins and the long QT syndrome;Van gen naar ziekte; Ionkanaaleiwitten en het lange-QT-intervalsyndroom

Nederlands Tijdschrift voor Geneeskunde

Volumn 144, Issue 46, 2000, Pages 2205-2207

  Wilde, A A M ^a   Van Langen, I M ^a  

^a ROYAL NETHERLANDS ACADEMY OF ARTS AND SCIENCES   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ION CHANNEL;

ELECTROCARDIOGRAM; GENE MUTATION; HEART REPOLARIZATION; HEART VENTRICLE ARRHYTHMIA; HUMAN; LONG QT SYNDROME; SHORT SURVEY; SUDDEN DEATH; SYNCOPE;

DEATH, SUDDEN, CARDIAC; ELECTROCARDIOGRAPHY; GENETIC SCREENING; HUMANS; ION CHANNEL GATING; ION CHANNELS; LONG QT SYNDROME; MEDICAL HISTORY TAKING; SYNCOPE; TACHYCARDIA, VENTRICULAR;

EID: 0034638739     PISSN: 00282162     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Short Survey

References (4)

1. Auditory stimuli as a trigger for arrhythmic events differentiate HERG-related (LQTS2) patients from KVLQT 1-related patients (LQTS1)
2. Gene-specific distribution of cardiac events in LQTS1 and LQTS2
3. Genetic and molecular basis of cardiac arrhythmias: Impact on clinical management. Study Group on molecular basis of arrhythmias of the Working Group on Arrhythmias of the European Society of Cardiology
4. Presymptomatisch onderzoek na plotselinge hartdood in de familie