Nav1.1 channels with mutations of severe myoclonic epilepsy in infancy display attenuated currents

Epilepsy Research

Volumn 54, Issue 2-3, 2003, Pages 201-207

  Sugawara, Takashi ^a   Tsurubuchi, Yuji ^a   Fujiwara, Tateki ^b   Mazaki Miyazaki, Emi ^a   Nagata, Keiichi ^a   Montal, Mauricio ^c   Inoue, Yushi ^b   Yamakawa, Kazuhiro ^a  

^a RIKEN BRAIN SCIENCE INSTITUTE   (Japan)

^b SHIZUOKA INSTITUTE OF EPILEPSY AND NEUROLOGICAL DISORDERS   (Japan)

^c NEUROBIOLOGY SECTION   (United States)

Author keywords

Mutations; Patch clamp; SCN1A; Severe myoclonic epilepsy in infancy; SMEI; Sodium channel

Indexed keywords

SODIUM CHANNEL; NERVE PROTEIN; SODIUM CHANNEL, VOLTAGE GATED, TYPE I, ALPHA PROTEIN; SODIUM CHANNEL, VOLTAGE-GATED, TYPE I, ALPHA PROTEIN;

ALPHA CHAIN; ARTICLE; CELL MUTANT; CELL STRAIN; CONTROLLED STUDY; DISEASE SEVERITY; HUMAN; HUMAN CELL; MISSENSE MUTATION; MYOCLONUS EPILEPSY; NONSENSE MUTATION; PATCH CLAMP; PHENOTYPE; PRIORITY JOURNAL; SODIUM CURRENT; CELL LINE; CHEMISTRY; GENETICS; MUTATION;

CELL LINE; EPILEPSIES, MYOCLONIC; HUMANS; MUTATION; NERVE TISSUE PROTEINS; SODIUM CHANNELS;

EID: 0038771150     PISSN: 09201211     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0920-1211(03)00084-6     Document Type: Article

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