New missense mutation (G626V) in the predicted selectivity filter of the HERG channel associated with familial long QT syndrome.

Human mutation

Volumn 15, Issue 6, 2000, Pages 584-

  Jahr, S ^a   Lewalter, T ^a   Hesch, R D ^a   Luderitz B ^a   Englisch, S ^a  

^a UNIVERSITY OF KONSTANZ   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

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

ARTICLE; GENETICS; HUMAN; LONG QT SYNDROME; MISSENSE MUTATION; MOLECULAR GENETICS;

CATION TRANSPORT PROTEINS; DNA-BINDING PROTEINS; ETHER-A-GO-GO POTASSIUM CHANNELS; GLYCINE; HUMANS; LONG QT SYNDROME; MOLECULAR SEQUENCE DATA; MUTATION, MISSENSE; POTASSIUM CHANNELS; POTASSIUM CHANNELS, VOLTAGE-GATED; TRANS-ACTIVATORS; VALINE;

EID: 0034201085     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/1098-1004(200006)15:6<584::AID-HUMU27>3.0.CO;2-L     Document Type: Article

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