A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

Cell

Volumn 80, Issue 5, 1995, Pages 795-803

  Curran, Mark E ^a   Splawski, Igor ^a   Timothy, Katherine W ^a   Vincen, G Michael ^a,c   Green, Eric D ^d   Keating, Mark T ^a,b  

^a UNIVERSITY OF UTAH HEALTH SCIENCES CENTER   (United States)

^b HOWARD HUGHES MEDICAL INSTITUTE   (United States)

^c Cardiology Division University Utah Health Sciences Center Salt Lake City ^*  (United States)

^d NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; MESSENGER RNA; POLYADENYLATED RNA; POTASSIUM CHANNEL;

ARTICLE; CHROMOSOME 11; CHROMOSOME 3; CHROMOSOME 7Q; CHROMOSOME MAP; DNA SEQUENCE; FEMALE; GENE DELETION; GENE EXPRESSION; GENE MUTATION; GENETIC LINKAGE; HEART ARRHYTHMIA; HUMAN; LONG QT SYNDROME; MAJOR CLINICAL STUDY; MALE; NORTHERN BLOTTING; PEDIGREE ANALYSIS; POINT MUTATION; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM; TORSADE DES POINTES; YEAST ARTIFICIAL CHROMOSOME;

AMINO ACID SEQUENCE; BASE SEQUENCE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 7; DNA MUTATIONAL ANALYSIS; FEMALE; GENETIC MARKERS; HUMAN; INTRONS; LONG QT SYNDROME; MALE; MOLECULAR SEQUENCE DATA; ORGAN SPECIFICITY; PEDIGREE; POINT MUTATION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; POTASSIUM CHANNELS; RNA, MESSENGER; SEQUENCE ANALYSIS, DNA; SEQUENCE DELETION; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0028914969     PISSN: 00928674     EISSN: None     Source Type: Journal    
DOI: 10.1016/0092-8674(95)90358-5     Document Type: Article

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