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Gene Expression Alterations in the Cerebellum and Granule Neurons of Cstb(−/−) Mouse Are Associated with Early Synaptic Changes and Inflammation
Progressive myoclonus epilepsy of Unverricht-Lundborg type (EPM1) is an autosomal recessively inherited neurodegenerative disease, manifesting with myoclonus, seizures and ataxia, caused by mutations in the cystatin B (CSTB) gene. With the aim of understanding the molecular basis of pathogenetic eve...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3937333/ https://www.ncbi.nlm.nih.gov/pubmed/24586687 http://dx.doi.org/10.1371/journal.pone.0089321 |