Analysis of common genetic variation across targets of microRNAs dysregulated both in ASD and epilepsy reveals negative correlation

Genetic overlap involving rare disrupting mutations may contribute to high comorbidity rates between autism spectrum disorders and epilepsy. Despite their polygenic nature, genome-wide association studies have not reported a significant contribution of common genetic variation to comorbidity between...

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Detalles Bibliográficos
Autores principales: Stella, Carol, Díaz-Caneja, Covadonga M., Penzol, Maria Jose, García-Alcón, Alicia, Solís, Andrea, Andreu-Bernabeu, Álvaro, Gurriarán, Xaquín, Arango, Celso, Parellada, Mara, González-Peñas, Javier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10034058/
https://www.ncbi.nlm.nih.gov/pubmed/36968597
http://dx.doi.org/10.3389/fgene.2023.1072563

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10034058/
https://www.ncbi.nlm.nih.gov/pubmed/36968597
http://dx.doi.org/10.3389/fgene.2023.1072563

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