Impaired osteoclast homeostasis in the cystatin B-deficient mouse model of progressive myoclonus epilepsy

Progressive myoclonus epilepsy of Unverricht–Lundborg type (EPM1) is an autosomal recessively inherited disorder characterized by incapacitating stimulus-sensitive myoclonus and tonic-clonic epileptic seizures with onset at the age of 6 to 16 years. EPM1 patients also exhibit a range of skeletal cha...

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Detalles Bibliográficos
Autores principales: Manninen, Otto, Puolakkainen, Tero, Lehto, Jemina, Harittu, Elina, Kallonen, Aki, Peura, Marko, Laitala-Leinonen, Tiina, Kopra, Outi, Kiviranta, Riku, Lehesjoki, Anna-Elina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5365244/
https://www.ncbi.nlm.nih.gov/pubmed/28377970
http://dx.doi.org/10.1016/j.bonr.2015.10.002

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5365244/
https://www.ncbi.nlm.nih.gov/pubmed/28377970
http://dx.doi.org/10.1016/j.bonr.2015.10.002

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