Delayed Postnatal Loss of P/Q-Type Calcium Channels Recapitulates the Absence Epilepsy, Dyskinesia, and Ataxia Phenotypes of Genomic Cacna1A Mutations

Inherited loss of P/Q-type calcium channel function causes human absence epilepsy, episodic dyskinesia, and ataxia, but the molecular “birthdate” of the neurological syndrome and its dependence on prenatal pathophysiology is unknown. Since these channels mediate transmitter release at synapses throu...

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Detalhes bibliográficos
Main Authors: Mark, Melanie D., Maejima, Takashi, Kuckelsberg, Denise, Yoo, Jong W., Hyde, Robert A., Shah, Viral, Gutierrez, Davina, Moreno, Rosa L., Kruse, Wolfgang, Noebels, Jeffrey L., Herlitze, Stefan
Formato: Artigo
Idioma:Inglês
Publicado em: Society for Neuroscience 2011
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3065835/
https://ncbi.nlm.nih.gov/pubmed/21411672
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.5342-10.2011
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