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dravet syndrome
(phenotype)
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Genetic Markers
Most Correlated Genes
Most Correlated SNPs
GABRG2
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
adult behavior
GSE1432_CTRL_VS_IFNG_1H_MICROGLIA_DN
GSE8921_UNSTIM_0H_VS_TLR1_2_STIM_MONOCYTE_3H_DN
Voltage gated sodium channel, alpha-1 subunit
Gamma-aminobutyric-acid A receptor, gamma 2 subunit
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Most Correlated Studies
Zebrafish larvae with Scn1a (Nav1.1) mutation
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Literature
Most Relevant Literature
Dravet syndrome (severe myoclonic epilepsy in infancy).
Hemiconvulsion-hemiplegia syndrome in a patient with severe myoclonic epilepsy in infancy.
Addition of verapamil in the treatment of severe myoclonic epilepsy in infancy.
Ictal vomiting as an initial symptom of severe myoclonic epilepsy in infancy: a case report.
Microchromosomal deletions involving SCN1A and adjacent genes in severe myoclonic epilepsy in infanc…
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Clinical Trials
Most Relevant Clinical Trials
Stiripentol in Dravet Syndrome
Treatment of Dravet Syndrome With Fenfluramine (Expanded Access Protocol)
Ataluren for Nonsense Mutation in CDKL5 and Dravet Syndrome
Compassionate Use of Stiripentol in Dravet Syndrome
Treatment of Gait Disorders in Children With Dravet Syndrome
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