Cystatin B knockout model of progressive myoclonus epilepsy: postnatal day 30 cerebellum - - GEO DataSets - NCBI

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Full record GDS5090

Cystatin B knockout model of progressive myoclonus epilepsy: postnatal day 30 cerebellum

Analysis of cerebella from symptomatic, postnatal day 30 cystatin B (CSTB)-deficient mice. Progressive myoclonus epilepsy of Unverricht-Lundborg type (EPM1) is a neurodegenerative disease caused by mutations in the CSTB gene. Results provide insight into the molecular basis of EPM1 pathogenesis.

Organism:: Mus musculus

Type:: Expression profiling by array, transformed count, 2 genotype/variation sets

Platform:: GPL1261
Series:: GSE47516
6 Samples

Download data: CEL

DataSet

Accession:: GDS5090

ID:: 5090

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Cystatin B knockout model of progressive myoclonus epilepsy: postnatal day 30 ce...
Cystatin B knockout model of progressive myoclonus epilepsy: postnatal day 30 cerebellum
Accession: GDS5090

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