Dissecting the phenotypes of Dravet syndrome by gene deletion

Brain

Volumn 138, Issue 8, 2015, Pages 2219-2233

  Rubinstein, Moran ^a   Han, Sung ^a   Tai, Chao ^a   Westenbroek, Ruth E ^a   Hunker, Avery ^a   Scheuer, Todd ^a   Catterall, William A ^a  

^a UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

Author keywords

Dravet syndrome; interneurons; Nav1.1; parvalbumin; sodium channel; somatostatin

Indexed keywords

PARVALBUMIN; SODIUM CHANNEL NAV1.1; SOMATOSTATIN; 4 AMINOBUTYRIC ACID RECEPTOR;

ACTION POTENTIAL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; AUTISM; BRAIN SLICE; COGNITIVE DEFECT; CONDITIONING; CONTROLLED STUDY; FEAR; FEMALE; GENE DELETION; HAPLOINSUFFICIENCY; HETEROZYGOTE; HIPPOCAMPAL CA1 REGION; HYPERACTIVITY; INTERNEURON; LONG TERM MEMORY; LOSS OF FUNCTION MUTATION; MALE; MOUSE; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; SEIZURE; SEIZURE SUSCEPTIBILITY; SEVERE MYOCLONIC EPILEPSY IN INFANCY; SHORT TERM MEMORY; SOCIAL INTERACTION; SPATIAL LEARNING; SPATIAL MEMORY; ANIMAL; EPILEPSIES, MYOCLONIC; EPILEPSY; GENETICS; HIPPOCAMPUS; METABOLISM; MUTATION; PATHOPHYSIOLOGY; PHYSIOLOGY;

ACTION POTENTIALS; ANIMALS; EPILEPSIES, MYOCLONIC; EPILEPSY; FEMALE; GABAERGIC NEURONS; GENE DELETION; HETEROZYGOTE; HIPPOCAMPUS; MALE; MICE; MUTATION; NAV1.1 VOLTAGE-GATED SODIUM CHANNEL; PHENOTYPE;

EID: 84940036844     PISSN: 00068950     EISSN: 14602156     Source Type: Journal    
DOI: 10.1093/brain/awv142     Document Type: Article

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