Leigh syndrome with atypical cerebellar lesions

Leigh Syndrome is a neurodegenerative disorder caused by mitochondrial dysfunction, with significant phenotypic and genetic heterogeneity. It usually presents in early life, with a severe prognosis. It can be caused by more than 75 different gene mutations, of nuclear and mitochondrial origin, invol...

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Detalles Bibliográficos
Autores principales: Veiga, Marcos Gil Alberto da, Marecos, Clara, Duarte, Sofia Temudo, Vieira, José Pedro, Conceição, Carla
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6614543/
https://www.ncbi.nlm.nih.gov/pubmed/31334367
http://dx.doi.org/10.1016/j.ensci.2019.100197

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6614543/
https://www.ncbi.nlm.nih.gov/pubmed/31334367
http://dx.doi.org/10.1016/j.ensci.2019.100197

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