Progressive Volume Loss and White Matter Degeneration in Cstb-Deficient Mice: A Diffusion Tensor and Longitudinal Volumetry MRI Study

Unverricht-Lundborg type progressive myoclonus epilepsy (EPM1, OMIM 254800) is an autosomal recessive disorder characterized by onset at the age of 6 to 16 years, incapacitating stimulus-sensitive myoclonus and tonic-clonic epileptic seizures. It is caused by mutations in the gene encoding cystatin...

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Detalles Bibliográficos
Autores principales: Manninen, Otto, Laitinen, Teemu, Lehtimäki, Kimmo K., Tegelberg, Saara, Lehesjoki, Anna-Elina, Gröhn, Olli, Kopra, Outi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3948351/
https://www.ncbi.nlm.nih.gov/pubmed/24603771
http://dx.doi.org/10.1371/journal.pone.0090709

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3948351/
https://www.ncbi.nlm.nih.gov/pubmed/24603771
http://dx.doi.org/10.1371/journal.pone.0090709

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