A recessive C-terminal Jervell and Lange-Nielsen mutation of the KCNQ1 channel impairs subunit assembly

EMBO Journal

Volumn 19, Issue 3, 2000, Pages 332-340

  Schmitt, Nicole ^a   Schwarz, Martin ^a   Peretz, Asher ^b   Abitbol, Ilane ^b   Attali, Bernard ^b   Pongs, Olaf ^a  

^a UNIVERSITY MEDICAL CENTER HAMBURG EPPENDORF   (Germany)

^b WEIZMANN INSTITUTE OF SCIENCE   (Israel)

Author keywords

K(v)LQT1 channels; Long QT syndrome; Potassium channels

Indexed keywords

POTASSIUM CHANNEL; PROTEIN SUBUNIT;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CARBOXY TERMINAL SEQUENCE; GENE LOCUS; GENE MUTATION; HUMAN; LONG QT SYNDROME; NONHUMAN; PRIORITY JOURNAL; PROTEIN ASSEMBLY; RECESSIVE GENE; SYNCOPE;

ANIMALIA; MUSTELA VISON;

EID: 0034141999     PISSN: 02614189     EISSN: None     Source Type: Journal    
DOI: 10.1093/emboj/19.3.332     Document Type: Article

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