Lafora progressive myoclonus epilepsy: NHLRC1 mutations affect glycogen metabolism

Lafora disease is a fatal autosomal recessive form of progressive myoclonus epilepsy. Patients manifest myoclonus and tonic–clonic seizures, visual hallucinations, intellectual, and progressive neurologic deterioration beginning in adolescence. The two genes known to be involved in Lafora disease ar...

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Detalles Bibliográficos
Autores principales: Couarch, Philippe, Vernia, Santiago, Gourfinkel-An, Isabelle, Lesca, Gaëtan, Gataullina, Svetlana, Fedirko, Estelle, Trouillard, Oriane, Depienne, Christel, Dulac, Olivier, Steschenko, Dominique, Leguern, Eric, Sanz, Pascual, Baulac, Stéphanie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2011
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3154284/
https://www.ncbi.nlm.nih.gov/pubmed/21505799
http://dx.doi.org/10.1007/s00109-011-0758-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3154284/
https://www.ncbi.nlm.nih.gov/pubmed/21505799
http://dx.doi.org/10.1007/s00109-011-0758-y

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