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The Ca(V)1.2 G406R mutation decreases synaptic inhibition and alters L-type Ca(2+) channel-dependent LTP at hippocampal synapses in a mouse model of Timothy Syndrome
Genetic alterations in autism spectrum disorders (ASD) frequently disrupt balance between synaptic excitation and inhibition and alter plasticity in the hippocampal CA1 region. Individuals with Timothy Syndrome (TS), a genetic disorder caused by Ca(V)1.2 L-type Ca(2+) channel (LTCC) gain-of function...
Autores principales: | Sanderson, Jennifer L., Freund, Ronald K., Castano, Anna M., Benke, Timothy A., Dell’Acqua, Mark L. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9644825/ https://www.ncbi.nlm.nih.gov/pubmed/36162529 http://dx.doi.org/10.1016/j.neuropharm.2022.109271 |
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