Gene-Expression Profiling Suggests Impaired Signaling via the Interferon Pathway in Cstb(-/-) Microglia

Progressive myoclonus epilepsy of Unverricht-Lundborg type (EPM1, OMIM254800) is an autosomal recessive neurodegenerative disorder characterized by stimulus-sensitive and action-activated myoclonus, tonic-clonic epileptic seizures, and ataxia. Loss-of-function mutations in the gene encoding the cyst...

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Detalles Bibliográficos
Autores principales: Körber, Inken, Katayama, Shintaro, Einarsdottir, Elisabet, Krjutškov, Kaarel, Hakala, Paula, Kere, Juha, Lehesjoki, Anna-Elina, Joensuu, Tarja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4927094/
https://www.ncbi.nlm.nih.gov/pubmed/27355630
http://dx.doi.org/10.1371/journal.pone.0158195

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4927094/
https://www.ncbi.nlm.nih.gov/pubmed/27355630
http://dx.doi.org/10.1371/journal.pone.0158195

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