Molecular diagnosis in a child with sudden infant death syndrome

Lancet

Volumn 358, Issue 9290, 2001, Pages 1342-1343

  Schwartz, Peter J ^a,b   Priori, Silvia G ^b,c   Bloise, Raffaella ^c   Napolitano, Carlo ^c   Ronchetti, Elena ^c   Piccinini, Andrea ^d   Goj, Carlo ^d   Breithardt, Günter ^e   Schulze Bahr, Eric ^e   Wedekind, Horst ^e   Nastoli, Janni ^c  

^a FONDAZIONE IRCCS POLICLINICO SAN MATTEO   (Italy)

^b UNIVERSITY OF PAVIA   (Italy)

^c IRCCS   (Italy)

^d UNIVERSITY OF MILAN   (Italy)

^e UNIVERSITY OF MÜNSTER   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; PROTEIN; PROTEIN KVLQT1; UNCLASSIFIED DRUG;

ARTICLE; CONTROLLED STUDY; ELECTROCARDIOGRAPHY; GENE; GENE MUTATION; GENETIC SCREENING; HUMAN; LONG QT SYNDROME; NEWBORN SCREENING; PRIORITY JOURNAL; SUDDEN INFANT DEATH SYNDROME;

EID: 0035922697     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(01)06450-9     Document Type: Article

References (5)

1. The sudden infant death syndrome: Cardio-respiratory mechanisms and interventions
2. Prolongation of the QT interval and the sudden infant death syndrome
3. A molecular link between the sudden infant death syndrome and the long QT syndrome
4. The long QT syndrome
5. QT prolongation and sudden infant death syndrome - From theory to evidence