Analysis of the human KCNH2(HERG) gene: identification and characterization of a novel mutation Y667X associated with long QT syndrome and a non-pathological 9 bp insertion.

Human mutation

Volumn 15, Issue 5, 2000, Pages 483-

  Paulussen, A ^a   Yang, P ^a   Pangalos, M ^a   Verhasselt, P ^a   Marrannes, R ^a   Verfaille, C ^a   Vandenberk, I ^a   Crabbe, R ^a   Konings, F ^a   Luyten, W ^a   Armstrong, M ^a  

^a JANSSEN RESEARCH FOUNDATION   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

CATION TRANSPORT PROTEIN; DNA BINDING PROTEIN; ERG PROTEIN, HUMAN; ERG1 POTASSIUM CHANNEL; KCNH2 PROTEIN, HUMAN; KCNH6 PROTEIN, HUMAN; POTASSIUM CHANNEL; POTASSIUM CHANNEL HERG; TRANSACTIVATOR PROTEIN; VOLTAGE GATED POTASSIUM CHANNEL;

ANIMAL; ARTICLE; CODON; ELECTROPHYSIOLOGY; GENE EXPRESSION REGULATION; GENETICS; HUMAN; LONG QT SYNDROME; PATCH CLAMP; PHYSIOLOGY; XENOPUS LAEVIS;

ANIMALS; CATION TRANSPORT PROTEINS; CODON; DNA-BINDING PROTEINS; ELECTROPHYSIOLOGY; ETHER-A-GO-GO POTASSIUM CHANNELS; HUMANS; LONG QT SYNDROME; MUTAGENESIS, INSERTIONAL; PATCH-CLAMP TECHNIQUES; POTASSIUM CHANNELS; POTASSIUM CHANNELS, VOLTAGE-GATED; TRANS-ACTIVATORS; XENOPUS LAEVIS;

MLCS; MLOWN;

EID: 0034184070     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/(sici)1098-1004(200005)15:5<483::aid-humu18>3.0.co;2-t     Document Type: Article

References (0)