Long QT syndrome-associated mutations in the voltage sensor of I Ks channels

Cellular Physiology and Biochemistry

Volumn 24, Issue 1-2, 2009, Pages 11-16

  Henrion, Ulrike ^a   Strutz Seebohm, Nathalie ^b   Duszenko, Michael ^a   Lang, Florian ^a   Seebohm, Guiscard ^a,b  

^a UNIVERSITY OF TÜBINGEN   (Germany)

^b RUHR UNIVERSITY BOCHUM   (Germany)

Author keywords

Arrhythmia; Cardiac action potential; Heart; KCNE; KCNQ; LQT

Indexed keywords

DELAYED RECTIFIER POTASSIUM CHANNEL; INTERMEDIATE CONDUCTANCE CALCIUM ACTIVATED POTASSIUM CHANNEL; POTASSIUM CHANNEL KCNE1; POTASSIUM CHANNEL KCNQ1;

ACTION POTENTIAL; AMINO ACID SUBSTITUTION; ANIMAL CELL; ARTICLE; ELECTRIC POTENTIAL; HUMAN; LONG QT SYNDROME; LONG QT SYNDROME 1; NEWBORN; NONHUMAN; NUCLEOTIDE SEQUENCE; OOCYTE; POTASSIUM CURRENT; PRIORITY JOURNAL; PROTEIN EXPRESSION; RAT; VOLTAGE CLAMP; XENOPUS LAEVIS;

EID: 67650462305     PISSN: 10158987     EISSN: None     Source Type: Journal    
DOI: 10.1159/000227828     Document Type: Article

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