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Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families
Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder with genetic and clinical heterogeneity. The interplay of de novo and inherited rare variants has been suspected in the development of ASD. Here, we applied whole exome sequencing (WES) on 19 trios from singleton Saudi families...
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| Pubblicato in: | Sci Rep |
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| Autori principali: | , , , , , , , , , , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Nature Publishing Group UK
2017
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5515956/ https://ncbi.nlm.nih.gov/pubmed/28720891 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-017-06033-1 |
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