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Analysing an allelic series of rare missense variants of CACNA1I in a Swedish schizophrenia cohort
CACNA1I is implicated in the susceptibility to schizophrenia by large-scale genetic association studies of single nucleotide polymorphisms. However, the channelopathy of CACNA1I in schizophrenia is unknown. CACNA1I encodes Ca(V)3.3, a neuronal voltage-gated calcium channel that underlies a subtype o...
Autores principales: | Baez-Nieto, David, Allen, Andrew, Akers-Campbell, Seth, Yang, Lingling, Budnik, Nikita, Pupo, Amaury, Shin, Young-Cheul, Genovese, Giulio, Liao, Maofu, Pérez-Palma, Eduardo, Heyne, Henrike, Lal, Dennis, Lipscombe, Diane, Pan, Jen Q. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9166571/ https://www.ncbi.nlm.nih.gov/pubmed/34919654 http://dx.doi.org/10.1093/brain/awab443 |
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