Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: Do we need a scoring system? [5]

European Heart Journal

Volumn 28, Issue 11, 2007, Pages 1399-

  Hofman, Nynke ^a   Wilde, Arthur A M ^a   Tan, Hanno L ^a  

^a ACADEMIC MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

DIAGNOSTIC PROCEDURE; GENETIC ANALYSIS; GENOTYPE; HUMAN; LETTER; LONG QT SYNDROME; MOLECULAR GENETICS; PHENOTYPE; PRIORITY JOURNAL; PUBLICATION; SCORING SYSTEM; SCREENING;

HUMANS; LONG QT SYNDROME; MOLECULAR DIAGNOSTIC TECHNIQUES;

EID: 34548404320     PISSN: 0195668X     EISSN: 15229645     Source Type: Journal    
DOI: 10.1093/eurheartj/ehm118     Document Type: Letter

References (2)

1. Rossenbacker T, Priori SG. Clinical diagnosis of long QT syndrome: back to the caliper. Eur Heart J 2007;28:527-528.
2. Hofman N, Wilde AAM, Kääb S, van Langen IM, Tanck MWT, Mannens MMAM, Hinterseer M, Beckmann B, Tan HL. Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system? Eur Heart J 2007;28:575-580.