K-aggravated myotonia mutations at residue G1306 differentially alter deactivation gating of human skeletal muscle sodium channels

Cellular and Molecular Neurobiology

Volumn 25, Issue 7, 2005, Pages 1075-1092

  Groome, James R ^a   Fujimoto, Esther ^b,c   Ruben, Peter C ^b  

^a IDAHO STATE UNIVERSITY   (United States)

^b UTAH STATE UNIVERSITY   (United States)

^c UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

Author keywords

Activation; Channelopathies; Deactivation; Gating; Inactivation; Mutations

Indexed keywords

POTASSIUM CHANNEL; VOLTAGE GATED SODIUM CHANNEL;

ARTICLE; CHANNEL GATING; CONTROLLED STUDY; ELECTRIC CURRENT; HYPERKALEMIA; HYPERPOLARIZATION; MUSCLE ACTION POTENTIAL; MUTATIONAL ANALYSIS; MYOTONIA; NONHUMAN; POTASSIUM CONDUCTANCE; PRIORITY JOURNAL; SKELETAL MUSCLE; STEADY STATE; VOLTAGE CLAMP; WILD TYPE;

ANIMALS; ELECTRIC CONDUCTIVITY; HUMANS; ION CHANNEL GATING; KINETICS; MUSCLE PROTEINS; MUSCLE, SKELETAL; MUTATION, MISSENSE; MYOTONIA; OOCYTES; SODIUM CHANNELS; TIME FACTORS; XENOPUS;

EID: 29944439488     PISSN: 02724340     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10571-005-8057-1     Document Type: Article

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