Minimal Change in the Cytoplasmic Calcium Dynamics in Striatal GABAergic Neurons of a DYT1 Dystonia Knock-In Mouse Model

DYT1 dystonia is the most common hereditary form of primary torsion dystonia. This autosomal-dominant disorder is characterized by involuntary muscle contractions that cause sustained twisting and repetitive movements. It is caused by an in-frame deletion in the TOR1A gene, leading to the deletion o...

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Detalles Bibliográficos
Autores principales: Iwabuchi, Sadahiro, Koh, Jin-Young, Wang, Kai, Ho, K. W. David, Harata, N. Charles
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3834333/
https://www.ncbi.nlm.nih.gov/pubmed/24260480
http://dx.doi.org/10.1371/journal.pone.0080793

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3834333/
https://www.ncbi.nlm.nih.gov/pubmed/24260480
http://dx.doi.org/10.1371/journal.pone.0080793

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