The long QT syndrome: A novel missense mutation in the S6 region of the KVLQT1 gene

Human Genetics

Volumn 100, Issue 3-4, 1997, Pages 356-361

  Van den Berg, Marcel H ^a,f   Wilde, Arthur A M ^b,c   Robles de Medina, E O ^b   Meyer, Henk ^a,d,f   Geelen, Jan L M C ^a,f   Jongbloed, Roselie J E ^d   Wellens, Hein J J ^e   Geraedts, Joep P M ^d  

^a MAASTRICHT UNIVERSITY   (Netherlands)

^b UTRECHT UNIVERSITY   (Netherlands)

^c ACADEMIC MEDICAL CENTER   (Netherlands)

^d Clinical Genetics Centre   (Netherlands)

^e MAASTRICHT UNIVERSITY MEDICAL CENTER   (Netherlands)

^f MAASTRICHT UNIVERSITY   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

POTASSIUM CHANNEL; SODIUM CHANNEL;

ARTICLE; CARBOXY TERMINAL SEQUENCE; CHROMOSOME 11P; CHROMOSOME 3P; CHROMOSOME 4Q; CHROMOSOME 7Q; CLINICAL ARTICLE; FEMALE; GENE LOCUS; HAPLOTYPE; HUMAN; LONG QT SYNDROME; MALE; MISSENSE MUTATION; PHENOTYPE; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM; SUDDEN DEATH; SYNCOPE;

DNA MUTATIONAL ANALYSIS; FEMALE; HUMANS; KCNQ POTASSIUM CHANNELS; KCNQ1 POTASSIUM CHANNEL; LINKAGE (GENETICS); LONG QT SYNDROME; MALE; MUTATION; PEDIGREE; POTASSIUM CHANNELS; POTASSIUM CHANNELS, VOLTAGE-GATED;

MUSTELA VISON;

EID: 0030924035     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050516     Document Type: Article

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