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Caytaxin Deficiency Disrupts Signaling Pathways in Cerebellar Cortex

The genetically dystonic (dt) rat, an autosomal recessive model of generalized dystonia, harbors an insertional mutation in Atcay. As a result, dt rats are deficient in Atcay transcript and the neuronally-restricted protein caytaxin. Previous electrophysiological and biochemical studies have defined...

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Bibliographic Details
Main Authors: Xiao, Jianfeng, Gong, Suzhen, LeDoux, Mark S.
Format: Artigo
Language:Inglês
Published: 2006
Subjects:
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC1868412/
https://ncbi.nlm.nih.gov/pubmed/17092653
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neuroscience.2006.09.042
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