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...

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Detalles Bibliográficos
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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Original Article
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

Internet

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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