Structure-function relationships of the disease-linked A218T oxytocin receptor variant

Various single nucleotide polymorphisms (SNPs) in the oxytocin receptor (OXTR) gene have been associated with behavioral traits, autism spectrum disorder (ASD) and other diseases. The non-synonymous SNP rs4686302 results in the OXTR variant A218T and has been linked to core characteristics of ASD, t...

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Detalles Bibliográficos
Autores principales: Meyer, Magdalena, Jurek, Benjamin, Alfonso-Prieto, Mercedes, Ribeiro, Rui, Milenkovic, Vladimir M., Winter, Julia, Hoffmann, Petra, Wetzel, Christian H., Giorgetti, Alejandro, Carloni, Paolo, Neumann, Inga D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9054668/
https://www.ncbi.nlm.nih.gov/pubmed/34980886
http://dx.doi.org/10.1038/s41380-021-01241-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9054668/
https://www.ncbi.nlm.nih.gov/pubmed/34980886
http://dx.doi.org/10.1038/s41380-021-01241-8

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