Fine Mapping of Dravet Syndrome Modifier Loci on Mouse Chromosomes 7 and 8. Survival data used for mapping are contained in this workbook. Contents: Sheet 1: Dsm2 / Chromosome 7 Survival Column A: a

DataCite Commons2024-05-03 更新50

Data for: Atypical myelinogenesis and reduced axon caliber in the Scn1a variant model of Dravet syndrome: An electron microscopy pilot study of developing and mature mouse corpus callosum.

Dravet综合征

髓鞘形成异常

Electron microscopy morphometric analysis raw data for the Scn1a gene variant model of Dravet syndrome and littermate controls aged P50 (n=4 per group).

NIAID Data Ecosystem40

Dravet syndrome in Sweden: a population-based study

Dravet综合征

流行病学

Dravet syndrome in Sweden: a population-based study

Global Health Data Exchange ()60

Differential gene expression in postnatal day 10 Scn1b+/+ vs. Scn1b -/- cortical layer VI

Dravet综合征

皮质类器官基因表达

Scn1b null mice are a model of a severe developmental and epileptic encephalopathy called Dravet Syndrome (DS). The goal of this study was to identify changes in gene expression between Scn1b wild-typ

NIAID Data Ecosystem40

Antisense oligonucleotides modulate aberrant inclusion of poison exons in SCN1A-related Dravet syndrome

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