Neuropathology of SCA34 showing widespread oligodendroglial pathology with vacuolar white matter degeneration: a case study

Spinocerebellar ataxia type 34 (SCA34) is an autosomal dominant inherited ataxia due to mutations in ELOVL4, which encodes one of the very long-chain fatty acid elongases. SCA38, another spinocerebellar ataxia, is caused by mutations in ELOVL5, a gene encoding another elongase. However, there have b...

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Detalles Bibliográficos
Autores principales: Ozaki, Kokoro, Irioka, Takashi, Uchihara, Toshiki, Yamada, Akane, Nakamura, Ayako, Majima, Takamasa, Igarashi, Susumu, Shintaku, Hiroshi, Yakeishi, Mayumi, Tsuura, Yukio, Okazaki, Yasushi, Ishikawa, Kinya, Yokota, Takanori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8543940/
https://www.ncbi.nlm.nih.gov/pubmed/34689836
http://dx.doi.org/10.1186/s40478-021-01272-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8543940/
https://www.ncbi.nlm.nih.gov/pubmed/34689836
http://dx.doi.org/10.1186/s40478-021-01272-w

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