Recessive gene disruptions in autism spectrum disorder

Autism spectrum disorder (ASD) affects up to 1 in 59 individuals(1). Genome-wide association and large-scale sequencing studies strongly implicate both common variants(2–4) and rare de novo variants(5–10) in ASD. Recessive mutations have also been implicated(11–14) but their contribution remains les...

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Bibliografiset tiedot
Julkaisussa:Nat Genet
Päätekijät: Doan, Ryan N, Lim, Elaine T., De Rubeis, Silvia, Betancur, Catalina, Cutler, David J., Chiocchetti, Andreas G., Overman, Lynne M., Soucy, Aubrie, Goetze, Susanne, Freitag, Christine M., Daly, Mark J., Walsh, Christopher A., Buxbaum, Joseph D., Yu, Timothy W.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2019
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6629034/
https://ncbi.nlm.nih.gov/pubmed/31209396
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41588-019-0433-8
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