Dopamine Receptor and Gα(olf) Expression in DYT1 Dystonia Mouse Models during Postnatal Development

BACKGROUND: DYT1 dystonia is a heritable, early-onset generalized movement disorder caused by a GAG deletion (ΔGAG) in the DYT1 gene. Neuroimaging studies and studies using mouse models suggest that DYT1 dystonia is associated with dopamine imbalance. However, whether dopamine imbalance is key to DY...

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Detalles Bibliográficos
Autores principales: Zhang, Lin, McCarthy, Deirdre M., Sharma, Nutan, Bhide, Pradeep G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4393110/
https://www.ncbi.nlm.nih.gov/pubmed/25860259
http://dx.doi.org/10.1371/journal.pone.0123104

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4393110/
https://www.ncbi.nlm.nih.gov/pubmed/25860259
http://dx.doi.org/10.1371/journal.pone.0123104

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