Mechanisms of cold sensitivity of paramyotonia congenita mutation R1448H and overlap syndrome mutation M1360V

Journal of Physiology

Volumn 547, Issue 3, 2003, Pages 691-698

  Mohammadi, Bahram ^a   Mitrovic, Nenad ^b   Lehmann Horn, Frank ^b   Dengler, Reinhard ^a   Bufler, Johannes ^a  

^a HANNOVER MEDICAL SCHOOL   (Germany)

^b UNIVERSITY OF ULM   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CELL PROTEIN; POTASSIUM ION; RECOMBINANT PROTEIN; SODIUM CHANNEL; SODIUM ION;

CELL MEMBRANE DEPOLARIZATION; CELL MEMBRANE POTENTIAL; CHANNEL GATING; COLD SENSATION; COLD SENSITIVITY; CONTROLLED STUDY; DISEASE SEVERITY; ELECTROPHYSIOLOGY; EMBRYO CELL; GENE ACTIVATION; GENE INACTIVATION; GENE MUTATION; HUMAN; HUMAN CELL; KIDNEY CELL; LOW TEMPERATURE; MISSENSE MUTATION; MUSCLE WEAKNESS; MYOTONIA; NEUROMUSCULAR DISEASE; PARALYSIS; PATCH CLAMP; PRIORITY JOURNAL; PROTEIN EXPRESSION; REVIEW; SKELETAL MUSCLE; SYMPTOMATOLOGY; TEMPERATURE DEPENDENCE; THOMSEN DISEASE; WILD TYPE;

CELL LINE; COLD; HUMANS; ION CHANNEL GATING; KIDNEY; MEMBRANE POTENTIALS; MUSCLE, SKELETAL; MUTATION, MISSENSE; MYOTONIC DISORDERS; PATCH-CLAMP TECHNIQUES; SODIUM; SODIUM CHANNELS;

EID: 0037444683     PISSN: 00223751     EISSN: None     Source Type: Journal    
DOI: 10.1113/jphysiol.2002.033928     Document Type: Review

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