Epilepsy in Leigh Syndrome With Mitochondrial DNA Mutations

Background: Leigh syndrome is a mitochondrial cytopathy that presents as a neurodegenerative disease with apparent manifestation in the central nervous system. The aim of the present study was to describe its dominant neurological clinical features and analyze data related to epilepsy in Leigh syndr...

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Detalles Bibliográficos
Autores principales: Lee, Sunho, Na, Ji-Hoon, Lee, Young-Mock
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6518976/
https://www.ncbi.nlm.nih.gov/pubmed/31139141
http://dx.doi.org/10.3389/fneur.2019.00496

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6518976/
https://www.ncbi.nlm.nih.gov/pubmed/31139141
http://dx.doi.org/10.3389/fneur.2019.00496

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