Differential Cerebellar GABA(A) Receptor Expression in Mice with Mutations in Ca(V)2.1 (P/Q-type) Calcium Channels

Ataxia is the predominant clinical manifestation of cerebellar dysfunction. Mutations in the human CACNA1A gene, encoding the pore-forming α(1) subunit of Ca(V)2.1 (P/Q-type) calcium channels, underlie several neurological disorders, including Episodic Ataxia type 2 and Familial Hemiplegic Migraine...

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Detalhes bibliográficos
Publicado no:Neuroscience
Main Authors: Kaja, Simon, Payne, Andrew J., Nielsen, Elsebet Ø., Thompson, Christopher L., van den Maagdenberg, Arn M.J.M., Koulen, Peter, Snutch, Terrance P.
Formato: Artigo
Idioma:Inglês
Publicado em: 2015
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4547859/
https://ncbi.nlm.nih.gov/pubmed/26208839
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neuroscience.2015.07.044
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