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Molecular mechanisms of epilepsyReduction of thalamic and cortical Ih by deletion of TRIP8b produces a mouse model of human absence epilepsy.Review: Hippocampal sclerosis in epilepsy: a neuropathology review.Mother and daughter with adolescent-onset severe frontal lobe dysfunction and epilepsy.Linkage analysis and exome sequencing identify a novel mutation in KCTD7 in patients with progressive myoclonus epilepsy with ataxia.
P2860
description
article científic
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article scientifique
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articol științific
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articolo scientifico
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artigo científico
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artigo científico
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artigo científico
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artikel ilmiah
@id
artikull shkencor
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artículo científico
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name
The molecular biology of genetic-based epilepsies.
@en
type
label
The molecular biology of genetic-based epilepsies.
@en
prefLabel
The molecular biology of genetic-based epilepsies.
@en
P2860
P1476
The molecular biology of genetic-based epilepsies
@en
P2093
P2860
P2888
P304
P356
10.1007/S12035-013-8523-6
P50
P577
2013-08-10T00:00:00Z
P6179
1049570412