Benign familial neonatal convulsions caused by altered gating of KCNQ2/KCNQ3 potassium channels.

The Journal of neuroscience : the official journal of the Society for Neuroscience

Volumn 22, Issue 2, 2002, Pages

  Castaldo, Pasqualina ^a   del Giudice, Emanuele Miraglia ^a   Coppola, Giangennaro ^a   Pascotto, Antonio ^a   Annunziato, Lucio ^a   Taglialatela, Maurizio ^a  

^a UNIVERSITY OF NAPLES FEDERICO II   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

KCNQ2 PROTEIN, HUMAN; KCNQ3 PROTEIN, HUMAN; POTASSIUM; POTASSIUM CHANNEL; POTASSIUM CHANNEL KCNQ2; POTASSIUM CHANNEL KCNQ3; PROTEIN SUBUNIT; VOLTAGE GATED POTASSIUM CHANNEL;

AMINO ACID SUBSTITUTION; ANIMAL; ARTICLE; BENIGN CHILDHOOD EPILEPSY; CELL CULTURE; CELL MEMBRANE; CHANNEL GATING; CYTOLOGY; DOMINANT GENE; GENE EXPRESSION; GENETICS; HUMAN; ITALY; METABOLISM; MICROINJECTION; MUTATION; OOCYTE; PATCH CLAMP; PATHOPHYSIOLOGY; PEDIGREE; PHYSIOLOGY; PROTEIN TERTIARY STRUCTURE; SITE DIRECTED MUTAGENESIS; STRUCTURE ACTIVITY RELATION; XENOPUS;

AMINO ACID SUBSTITUTION; ANIMALS; CELL MEMBRANE; CELLS, CULTURED; EPILEPSY, BENIGN NEONATAL; GENE EXPRESSION; GENES, DOMINANT; HUMANS; ION CHANNEL GATING; ITALY; KCNQ2 POTASSIUM CHANNEL; KCNQ3 POTASSIUM CHANNEL; MICROINJECTIONS; MUTAGENESIS, SITE-DIRECTED; MUTATION; OOCYTES; PATCH-CLAMP TECHNIQUES; PEDIGREE; POTASSIUM; POTASSIUM CHANNELS; POTASSIUM CHANNELS, VOLTAGE-GATED; PROTEIN STRUCTURE, TERTIARY; PROTEIN SUBUNITS; STRUCTURE-ACTIVITY RELATIONSHIP; XENOPUS;

MLCS; MLOWN;

EID: 0037082188     PISSN: None     EISSN: 15292401     Source Type: Journal    
DOI: 10.1523/jneurosci.22-02-j0003.2002     Document Type: Article

References (0)