The Long Noncoding RNA RPS10P2-AS1 Is Implicated in Autism Spectrum Disorder Risk and Modulates Gene Expression in Human Neuronal Progenitor Cells

Most of the genetic risk for autism spectrum disorder (ASD) is inherited as common genetic variants, although some rare mutations have been identified in individuals with ASD. Common genetic variants are most parsimoniously identified by genome wide association studies. Genome wide association studi...

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Detalles Bibliográficos
Autores principales: Bilinovich, Stephanie M., Lewis, Kristy, Grepo, Nicole, Campbell, Daniel B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6804435/
https://www.ncbi.nlm.nih.gov/pubmed/31681417
http://dx.doi.org/10.3389/fgene.2019.00970

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6804435/
https://www.ncbi.nlm.nih.gov/pubmed/31681417
http://dx.doi.org/10.3389/fgene.2019.00970

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