Neuropathological hallmarks in autopsied cases with mitochondrial diseases caused by the mitochondrial 3243A>G mutation

The mitochondrial (m.) 3243A>G mutation is known to be associated with various mitochondrial diseases including mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke‐like episodes (MELAS). Their clinical symptoms have been estimated to occur with an increased mitochondrial DNA (mtDN...

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Detalles Bibliográficos
Autores principales: Miyahara, Hiroaki, Tamai, Chisato, Inoue, Masanori, Sekiguchi, Kazuhito, Tahara, Daisuke, Tahara, Nao, Takeda, Kazuhiro, Arafuka, Shusei, Moriyoshi, Hideyuki, Koizumi, Ryuichi, Akagi, Akio, Riku, Yuichi, Sone, Jun, Yoshida, Mari, Ihara, Kenji, Iwasaki, Yasushi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10580013/
https://www.ncbi.nlm.nih.gov/pubmed/37534760
http://dx.doi.org/10.1111/bpa.13199

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