Derivation of spinocerebellar ataxia type 3 human embryonic stem cell line UMICHe001-A/UM134-1

The most common autosomal dominant ataxia worldwide, spinocerebellar ataxia type 3 (SCA3) is a fatal, progressive neurodegenerative disorder caused by a CAG trinucleotide repeat expansion in the ATXN3 gene. Here we report the generation of human embryonic stem cell (hESC) line UM134-1, the first SCA...

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Detalles Bibliográficos
Autores principales: Moore, Lauren R., Keller, Laura, Paulson, Henry L., Smith, Gary D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10020865/
https://www.ncbi.nlm.nih.gov/pubmed/35952620
http://dx.doi.org/10.1016/j.scr.2022.102873

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10020865/
https://www.ncbi.nlm.nih.gov/pubmed/35952620
http://dx.doi.org/10.1016/j.scr.2022.102873

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