Dynamic nuclear envelope phenotype in rats overexpressing mutated human torsinA protein

A three-base-pair deletion in the human TOR1A gene is causative for the most common form of primary dystonia: the early-onset dystonia type 1 (DYT1 dystonia). The pathophysiological consequences of this mutation are still unknown. To study the pathology of the mutant torsinA (TOR1A) protein, we have...

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Detalles Bibliográficos
Autores principales: Yu-Taeger, Libo, Gaiser, Viktoria, Lotzer, Larissa, Roenisch, Tina, Fabry, Benedikt Timo, Stricker-Shaver, Janice, Casadei, Nicolas, Walter, Michael, Schaller, Martin, Riess, Olaf, Nguyen, Huu Phuc, Ott, Thomas, Grundmann-Hauser, Kathrin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6078351/
https://www.ncbi.nlm.nih.gov/pubmed/29739751
http://dx.doi.org/10.1242/bio.032839

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6078351/
https://www.ncbi.nlm.nih.gov/pubmed/29739751
http://dx.doi.org/10.1242/bio.032839

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