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Altered Cav1.2 function in the Timothy Syndrome mouse model produces ascending serotonergic abnormalities
Polymorphism in the gene CACNA1C, encoding the pore-forming subunit of Cav1.2 L-type calcium channels, has one of the strongest genetic linkages to schizophrenia, bipolar disorder, and major depressive disorder: psychopathologies in which serotonin signaling has been implicated. Additionally, a gain...
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| Publicado no: | Eur J Neurosci |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5640497/ https://ncbi.nlm.nih.gov/pubmed/28921675 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/ejn.13707 |
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