Electrophysiological properties of the hypokalaemic periodic paralysis mutation (R528H) of the skeletal muscle α1S subunit as expressed in mouse L cells

FEBS Letters

Volumn 382, Issue 3, 1996, Pages 244-248

  Lapie, Pascale ^a   Goudet, Cyril ^b   Nargeot, Joël ^b   Fontaine, Bertrand ^a   Lory, Philippe ^b  

^a PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^b Centre National de la Recherche Scientifique   (France)

Author keywords

Hypokalaemic periodic paralysis; L type Ca2+ channel; Mouse L cell; Skeletal 1 subunit; Transfection

Indexed keywords

1,4 DIHYDRO 2,6 DIMETHYL 5 NITRO 4 [2 (TRIFLUOROMETHYL)PHENYL] 3 PYRIDINECARBOXYLIC ACID METHYL ESTER; CALCIUM CHANNEL;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; DNA TRANSFER; DRUG SENSITIVITY; ELECTROPHYSIOLOGY; GENE EXPRESSION; L CELL; MOUSE; NONHUMAN; PERIODIC PARALYSIS; POINT MUTATION; PRIORITY JOURNAL; RABBIT;

ANIMALS; BARIUM; BASE SEQUENCE; CALCIUM CHANNELS; CALCIUM CHANNELS, L-TYPE; ELECTROPHYSIOLOGY; ION TRANSPORT; L CELLS (CELL LINE); MICE; MOLECULAR SEQUENCE DATA; MUSCLE, SKELETAL; PARALYSES, FAMILIAL PERIODIC; POINT MUTATION; RABBITS; TRANSFECTION;

EID: 0029985820     PISSN: 00145793     EISSN: None     Source Type: Journal    
DOI: 10.1016/0014-5793(96)00173-1     Document Type: Article

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