SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

Cell

Volumn 80, Issue 5, 1995, Pages 805-811

  Wang, Qing ^a,b   Shen, Jiaxiang ^a,b   Splawski, Igor ^b   Atkinson, Donald ^a,b   Li, Zhizhong ^b   Robinson, Jennifer L ^c   Moss, Arthur J ^d   Towbin, Jeffrey A ^e   Keating, Mark T ^a,b  

^a HOWARD HUGHES MEDICAL INSTITUTE   (United States)

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

^c Departments of Family Medicine   (United States)

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

^e BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; SODIUM CHANNEL;

AMINO ACID SEQUENCE; ARTICLE; CHROMOSOME MAP; DNA SEQUENCE; FEMALE; GENE DELETION; GENE MUTATION; GENETIC LINKAGE; HEART ARRHYTHMIA; HEART VENTRICLE FIBRILLATION; HUMAN; LONG QT SYNDROME; MAJOR CLINICAL STUDY; MALE; PEDIGREE ANALYSIS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM; TORSADE DES POINTES;

AMINO ACID SEQUENCE; BASE SEQUENCE; CLONING, MOLECULAR; DNA MUTATIONAL ANALYSIS; FEMALE; HUMAN; LINKAGE (GENETICS); LONG QT SYNDROME; MALE; MOLECULAR SEQUENCE DATA; PEDIGREE; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; SEQUENCE DELETION; SODIUM CHANNELS; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0028905566     PISSN: 00928674     EISSN: None     Source Type: Journal    
DOI: 10.1016/0092-8674(95)90359-3     Document Type: Article

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