Dravet syndrome: insights from in vitro experimental models.
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Dravet syndrome patient-derived neurons suggest a novel epilepsy mechanism.Nonfunctional NaV1.1 familial hemiplegic migraine mutant transformed into gain of function by partial rescue of folding defectsDo seizures and epileptic activity worsen epilepsy and deteriorate cognitive function?Pure haploinsufficiency for Dravet syndrome Na(V)1.1 (SCN1A) sodium channel truncating mutations.
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Dravet syndrome: insights from in vitro experimental models.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on April 2011
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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Dravet syndrome: insights from in vitro experimental models.
@en
Dravet syndrome: insights from in vitro experimental models.
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type
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Dravet syndrome: insights from in vitro experimental models.
@en
Dravet syndrome: insights from in vitro experimental models.
@nl
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Dravet syndrome: insights from in vitro experimental models.
@en
Dravet syndrome: insights from in vitro experimental models.
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P2860
P1433
P1476
Dravet syndrome: insights from in vitro experimental models
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P2093
Massimo Mantegazza
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P356
10.1111/J.1528-1167.2011.03005.X
P478
52 Suppl 2
P577
2011-04-01T00:00:00Z