Co-occurrence of amyotrophic lateral sclerosis and Leber’s hereditary optic neuropathy: is mitochondrial dysfunction a modifier?

Detalles Bibliográficos
Autores principales: Amore, Giulia, Vacchiano, Veria, La Morgia, Chiara, Valentino, Maria L., Caporali, Leonardo, Fiorini, Claudio, Ormanbekova, Danara, Salvi, Fabrizio, Bartoletti-Stella, Anna, Capellari, Sabina, Liguori, Rocco, Carelli, Valerio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Letter to the Editors
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9813087/
https://www.ncbi.nlm.nih.gov/pubmed/36066624
http://dx.doi.org/10.1007/s00415-022-11355-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9813087/
https://www.ncbi.nlm.nih.gov/pubmed/36066624
http://dx.doi.org/10.1007/s00415-022-11355-w

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