IsK and KvLQT1: Mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndrome

Human Molecular Genetics

Volumn 6, Issue 12, 1997, Pages 2179-2185

  Tyson, Jessica ^a   Tranebjærg, Lisbeth ^b   Bellman, Sue ^c   Wren, Christopher ^c   Taylor, James F N ^c   Bathen, Jørn ^d   Aslaksen, Bjørn ^e   Sørland, Svein Jan ^f   Lund, Ole ^g   Malcolm, Sue ^a   Pembrey, Marcus ^a   Bhattacharya, Shomi ^h   Bitner Glindzicz, Maria ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b UNIVERSITY HOSPITAL OF NORTH NORWAY   (Norway)

^c ROYAL FREE AND UNIVERSITY COLLEGE MEDICAL SCHOOL   (United Kingdom)

^d TRONDHEIM UNIVERSITY HOSPITAL   (Norway)

^e Central Hospital   (Norway)

^f OSLO UNIVERSITY HOSPITAL   (Norway)

^g Namdal Hospital   (Norway)

^h UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

MEMBRANE PROTEIN; POTASSIUM CHANNEL; PROTEIN SUBUNIT;

ARTICLE; CHROMOSOME 21; CLINICAL ARTICLE; CONSANGUINITY; GENE; GENE LOCUS; GENE MUTATION; GENETIC HETEROGENEITY; GENETIC MARKER; HUMAN; HUMAN CELL; LONG QT SYNDROME; PRIORITY JOURNAL;

CHROMOSOMES, HUMAN, PAIR 21; DELAYED RECTIFIER POTASSIUM CHANNELS; FEMALE; HUMANS; KCNQ POTASSIUM CHANNELS; KCNQ1 POTASSIUM CHANNEL; LINKAGE (GENETICS); LONG QT SYNDROME; MALE; MUTATION; PEDIGREE; POTASSIUM CHANNELS; POTASSIUM CHANNELS, VOLTAGE-GATED;

EID: 9844261701     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/6.12.2179     Document Type: Article

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