KVLQT1 mutations in three families with familial or sporadic long QT syndrome

Human Molecular Genetics

Volumn 5, Issue 9, 1996, Pages 1319-1324

  Russell, Mark W ^a   Dick II, Macdonald ^a   Collins, Francis S ^a   Brody, Lawrence C ^a  

^a UNIVERSITY OF MICHIGAN   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALANINE; POTASSIUM CHANNEL; VALINE;

AMINO ACID SUBSTITUTION; ARTICLE; CLINICAL ARTICLE; FAMILIAL DISEASE; FAMILY STUDY; GENE MUTATION; HUMAN; HUMAN CELL; LONG QT SYNDROME; MISSENSE MUTATION; PHENOTYPE; POTASSIUM CURRENT; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM;

AMINO ACID SEQUENCE; CHROMOSOMES, HUMAN, PAIR 11; HAPLOTYPES; HUMANS; LINKAGE (GENETICS); LONG QT SYNDROME; MOLECULAR SEQUENCE DATA; MUTATION; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL;

EID: 0029840732     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/5.9.1319     Document Type: Article

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