A recessive variant of the Romano-Ward long-QT syndrome?

Circulation

Volumn 97, Issue 24, 1998, Pages 2420-2425

  Priori, Silvia G ^a,b,c   Schwartz, Peter J ^c,d   Napolitano, Carlo ^a,b,d   Bianchi, Laura ^e   Dennis, Adrienne ^e   De Fusco, Maurizio ^a   Brown, Arthur M ^e   Casari, Giorgio ^a  

^a TELETHON INSTITUTE OF GENETICS AND MEDICINE TIGEM   (Italy)

^b IRCCS   (Italy)

^c UNIVERSITY OF PAVIA   (Italy)

^d UNIVERSITY OF MILAN   (Italy)

^e CASE WESTERN RESERVE UNIVERSITY   (United States)

Author keywords

Arrhythmia; Death, sudden; Genetics; Molecular biology; Torsade de pointes

Indexed keywords

ALANINE; COMPLEMENTARY RNA; THREONINE;

AMINO ACID SUBSTITUTION; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CASE REPORT; CONSANGUINITY; DOMINANT INHERITANCE; GENETIC PREDISPOSITION; HEART REPOLARIZATION; HEART VENTRICLE ARRHYTHMIA; HOMOZYGOSITY; HUMAN; HUMAN CELL; LONG QT SYNDROME; MALE; MISSENSE MUTATION; PHENOTYPE; PRIORITY JOURNAL; SCHOOL CHILD;

EID: 0032560610     PISSN: 00097322     EISSN: None     Source Type: Journal    
DOI: 10.1161/01.CIR.97.24.2420     Document Type: Article

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