A novel mutation in KVLQT1 is the molecular basis of inherited long QT syndrome in a near-drowning patient's family

Pediatric Research

Volumn 44, Issue 2, 1998, Pages 148-153

  Ackerman, Michael J ^a,b   Schroeder, Jennier J ^a   Berry, Rebecca ^a   Schaid, Daniel J ^a   Porter, Co Burn J ^a   Michels, Virginia V ^a   Thibodeau, Stephen N ^a  

^a MAYO CLINIC   (United States)

^b Mayo Eugenio Litta Children's Hospital   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ION CHANNEL;

ARTICLE; CASE REPORT; CHILD; CHROMOSOME 11P; CLINICAL FEATURE; ELECTROCARDIOGRAM; GENE DELETION; GENE ISOLATION; HUMAN; LONG QT SYNDROME; MALE; NEAR DROWNING; PEDIGREE; PRIORITY JOURNAL; SCHOOL CHILD;

EID: 0031848178     PISSN: 00313998     EISSN: None     Source Type: Journal    
DOI: 10.1203/00006450-199808000-00002     Document Type: Article

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