A novel sodium channel mutation causing a hyperkalemic paralytic and paramyotonic syndrome with variable clinical expressivity

Neurology

Volumn 49, Issue 4, 1997, Pages 1018-1025

  Wagner, S ^a,b,c   Lerche, H ^a,b,c   Mitrovic, N ^a,b,c   Heine, R ^a,b,c   George, A L ^a,b,c   Lehmann Horn, F ^a,b,c  

^a Institute of Applied Physiology   (Germany)

^b UNIVERSITY OF ULM   (Germany)

^c VANDERBILT UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

SODIUM CHANNEL;

ARTICLE; CHANNEL GATING; GENE MUTATION; HUMAN; HUMAN TISSUE; MUSCLE WEAKNESS; PERIODIC PARALYSIS; POINT MUTATION; PRIORITY JOURNAL; THOMSEN DISEASE;

EID: 0030697470     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.49.4.1018     Document Type: Article

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