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Autism-like phenotype and risk gene-RNA deadenylation by CPEB4 mis-splicing
Common genetic contributions to autism spectrum disorder (ASD) reside in risk-gene variants that individually have minimal effect-sizes. Since neurodevelopment-perturbing environmental factors also underlie idiopathic-ASD, it is crucial to identify altered regulators able to orchestrate multiple ASD...
Autores principales: | Parras, Alberto, Anta, Héctor, Santos-Galindo, María, Swarup, Vivek, Elorza, Ainara, Nieto-Gonzalez, José L., Picó, Sara, Hernández, Ivó H., Díaz-Hernández, Juan I., Belloc, Eulàlia, Rodolosse, Annie, Parikshak, Neelroop N., Peñagarikano, Olga, Fernández-Chacón, Rafael, Irimia, Manuel, Navarro, Pilar, Geschwind, Daniel H., Méndez, Raúl, Lucas, José J. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6217926/ https://www.ncbi.nlm.nih.gov/pubmed/30111840 http://dx.doi.org/10.1038/s41586-018-0423-5 |
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