Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current

Proceedings of the National Academy of Sciences of the United States of America

Volumn 97, Issue 17, 2000, Pages 9549-9554

  Jurkat Rott, Karin ^a   Mitrovic, Nenad ^a   Hang, Chao ^a   Kouzmekine, Alexei ^a   Iaizzo, Paul ^a,b   Herzog, Jürgen ^a,c   Lerche, Holger ^a   Nicole, Sophie ^d   Vale Santos, Jose ^e   Chauveau, Dominique ^f   Fontaine, Bertrand ^d   Lehmann Horn, Frank ^a  

^a UNIVERSITY OF ULM   (Germany)

^b UNIVERSITY OF MINNESOTA   (United States)

^c UNIVERSITY OF MUNICH   (Germany)

^d PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^e Department of Neurology ^*  (Portugal)

^f HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

Channelopathy; Functional expression; Molecular genetics; Muscle disease

Indexed keywords

SODIUM CHANNEL;

ADULT; ARTICLE; CLINICAL ARTICLE; FAMILY STUDY; FEMALE; GENE MUTATION; GENETIC LINKAGE; HUMAN; HUMAN TISSUE; HYPOKALEMIC PERIODIC PARALYSIS; MALE; MEMBRANE CONDUCTANCE; MEMBRANE STEADY POTENTIAL; MUSCLE FORCE; MUSCLE POTENTIAL; NUCLEOTIDE SEQUENCE; PEDIGREE; PRIORITY JOURNAL;

EID: 0040565182     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.97.17.9549     Document Type: Article

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