Enhanced inactivation and pH sensitivity of Na+ channel mutations causing hypokalaemic periodic paralysis type II

Brain

Volumn 125, Issue 4, 2002, Pages 835-843

  Kuzmenkin, Alexey ^a   Muncan, Vanesa ^a   Jurkat Rott, Karin ^a   Hang, Chao ^a   Lerche, Holger ^a   Lehmann Horn, Frank ^a   Mitrovic, Nenad ^a  

^a UNIVERSITY OF ULM   (Germany)

Author keywords

Channelopathies; Paralysis; Patch clamp; S4 segment; Voltage sensor

Indexed keywords

ACETAZOLAMIDE; ARGININE; CALCIUM CHANNEL; GENE PRODUCT; GLYCINE; HISTIDINE; SERINE; SODIUM ION;

AMINO ACID SUBSTITUTION; ARTICLE; BRAIN ELECTROPHYSIOLOGY; CACNA1S GENE; CASE REPORT; CHANNEL GATING; GENE ISOLATION; GENE MUTATION; GENETIC ANALYSIS; HUMAN; HYPOKALEMIC PERIODIC PARALYSIS; MEMBRANE STEADY POTENTIAL; MUSCLE CELL; MUSCLE DISEASE; MUSCLE WEAKNESS; PARALYSIS; PATCH CLAMP; PATHOPHYSIOLOGY; PH; PHYSICAL ACTIVITY; PRIORITY JOURNAL; SENSOR; SODIUM TRANSPORT; VOLTAGE CLAMP;

EID: 0036211354     PISSN: 00068950     EISSN: None     Source Type: Journal    
DOI: 10.1093/brain/awf071     Document Type: Article

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