Quantitative Changes in the Mitochondrial Proteome of Cerebellar Synaptosomes From Preclinical Cystatin B-Deficient Mice

Progressive myoclonus epilepsy of Unverricht-Lundborg type (EPM1) is a neurodegenerative disorder caused by loss-of-function mutations in the cystatin B (CSTB) gene. Progression of the clinical symptoms in EPM1 patients, including stimulus-sensitive myoclonus, tonic-clonic seizures, and ataxia, are...

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Detalles Bibliográficos
Autores principales: Gorski, Katarin, Spoljaric, Albert, Nyman, Tuula A., Kaila, Kai, Battersby, Brendan J., Lehesjoki, Anna-Elina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7691638/
https://www.ncbi.nlm.nih.gov/pubmed/33281550
http://dx.doi.org/10.3389/fnmol.2020.570640

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7691638/
https://www.ncbi.nlm.nih.gov/pubmed/33281550
http://dx.doi.org/10.3389/fnmol.2020.570640

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