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L-type calcium channels and neuropsychiatric diseases: Insights into genetic risk variant-associated genomic regulation and impact on brain development

Recent human genetic studies have linked a variety of genetic variants in the CACNA1C and CACNA1D genes to neuropsychiatric and neurodevelopmental disorders. This is not surprising given the work from multiple laboratories using cell and animal models that have established that Ca(v)1.2 and Ca(v)1.3...

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Detalles Bibliográficos
Autores principales: Baker, Madelyn R., Lee, Andrew S., Rajadhyaksha, Anjali M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9980663/
https://www.ncbi.nlm.nih.gov/pubmed/36803254
http://dx.doi.org/10.1080/19336950.2023.2176984