Behavioral and Electrophysiological Characterization of Dyt1 Heterozygous Knockout Mice

DYT1 dystonia is an inherited movement disorder caused by mutations in DYT1 (TOR1A), which codes for torsinA. Most of the patients have a trinucleotide deletion (ΔGAG) corresponding to a glutamic acid in the C-terminal region (torsinA(ΔE)). Dyt1 ΔGAG heterozygous knock-in (KI) mice, which mimic ΔGAG...

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Detalhes bibliográficos
Publicado no:PLoS One
Main Authors: Yokoi, Fumiaki, Chen, Huan-Xin, Dang, Mai Tu, Cheetham, Chad C., Campbell, Susan L., Roper, Steven N., Sweatt, J. David, Li, Yuqing
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2015
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4370625/
https://ncbi.nlm.nih.gov/pubmed/25799505
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0120916
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