Novel KCNQ1 and HERG missense mutations in Dutch long-QT families

Human Mutation

Volumn 13, Issue 4, 1999, Pages 301-310

  Jongbloed, R J E ^e   Wilde, A A M ^a,b   Geelen, J L M C ^f   Doevendans, P ^f   Schaap, C ^f   Van Langen, I ^a   Van Tintelen, J P ^b   Cobben, J M ^c   Beaufort Krol, G C M ^d   Geraedts, J P M ^f   Smeets, H J M ^f  

^a ACADEMIC MEDICAL CENTER   (Netherlands)

^b UTRECHT UNIVERSITY   (Netherlands)

^c UNIVERSITY OF GRONINGEN   (Netherlands)

^d UNIVERSITY MEDICAL CENTER GRONINGEN   (Netherlands)

^e MAASTRICHT UNIVERSITY   (Netherlands)

^f NONE

Author keywords

Arrhythmia; HERG; KCNQ1; Long QT; Mutation detection; Potassium channel

Indexed keywords

POTASSIUM CHANNEL;

ARTICLE; AUDITORY STIMULATION; DNA DETERMINATION; ELECTROCARDIOGRAM; FAMILY STUDY; GENE LOCUS; HEART ARRHYTHMIA; HEART VENTRICLE ARRHYTHMIA; HUMAN; LONG QT SYNDROME; MISSENSE MUTATION; NETHERLANDS; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; QT INTERVAL;

CATION TRANSPORT PROTEINS; DNA MUTATIONAL ANALYSIS; DNA-BINDING PROTEINS; ETHER-A-GO-GO POTASSIUM CHANNELS; HAPLOTYPES; HUMANS; KCNQ POTASSIUM CHANNELS; KCNQ1 POTASSIUM CHANNEL; LINKAGE (GENETICS); LONG QT SYNDROME; MICROSATELLITE REPEATS; MUTATION, MISSENSE; NETHERLANDS; PEDIGREE; POLYMORPHISM, GENETIC; POTASSIUM CHANNELS; POTASSIUM CHANNELS, VOLTAGE-GATED; SEQUENCE HOMOLOGY, AMINO ACID; TRANS-ACTIVATORS;

EID: 0032982314     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-1004(1999)13:4<301::AID-HUMU7>3.0.CO;2-V     Document Type: Article

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