Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorder

More than 98% of the human genome is made up of non-coding DNA, but techniques to ascertain its contribution to human disease have lagged far behind our understanding of protein coding variations. Autism spectrum disorder (ASD) has been mostly associated with coding variations via de novo single nuc...

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Detalles Bibliográficos
Autores principales: Schmitz-Abe, Klaus, Sanchez-Schmitz, Guzman, Doan, Ryan N., Hill, R. Sean, Chahrour, Maria H., Mehta, Bhaven K., Servattalab, Sarah, Ataman, Bulent, Lam, Anh-Thu N., Morrow, Eric M., Greenberg, Michael E., Yu, Timothy W., Walsh, Christopher A., Markianos, Kyriacos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7441318/
https://www.ncbi.nlm.nih.gov/pubmed/32820185
http://dx.doi.org/10.1038/s41598-020-70656-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7441318/
https://www.ncbi.nlm.nih.gov/pubmed/32820185
http://dx.doi.org/10.1038/s41598-020-70656-0

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