Sodium channel mutations in paramyotonia congenita uncouple inactivation from activation

Neuron

Volumn 12, Issue 2, 1994, Pages 281-294

  Chahine, Mohamed ^a   George Jr , Alfred L ^b   Zhou, Ming ^b   Ji, Sen ^c   Sun, Weijing ^c   Barchi, Robert L ^c   Horn, Richard ^a  

^a THOMAS JEFFERSON UNIVERSITY   (United States)

^b VANDERBILT UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

SODIUM CHANNEL;

AMINO ACID SUBSTITUTION; ARTICLE; GENE MUTATION; HUMAN; HUMAN CELL; MUSCLE CONTRACTION; NERVE CONDUCTION; PRIORITY JOURNAL; SODIUM CURRENT; THOMSEN DISEASE;

BASE SEQUENCE; ELECTROPHYSIOLOGY; EXTRACELLULAR SPACE; HUMAN; HYDROGEN-ION CONCENTRATION; MOLECULAR SEQUENCE DATA; MUTATION; MYOTONIA CONGENITA; POINT MUTATION; REACTION TIME; SODIUM CHANNELS; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.; TEMPERATURE;

EID: 0028326016     PISSN: 08966273     EISSN: None     Source Type: Journal    
DOI: 10.1016/0896-6273(94)90271-2     Document Type: Article

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