An integrated analysis of rare CNV and exome variation in Autism Spectrum Disorder using the Infinium PsychArray

Autism spectrum disorder (ASD) is a neurodevelopmental condition with a complex and heterogeneous genetic etiology. While a proportion of ASD risk is attributable to common variants, rare copy-number variants (CNVs) and protein-disrupting single-nucleotide variants (SNVs) have been shown to signific...

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Detalles Bibliográficos
Autores principales: Bacchelli, Elena, Cameli, Cinzia, Viggiano, Marta, Igliozzi, Roberta, Mancini, Alice, Tancredi, Raffaella, Battaglia, Agatino, Maestrini, Elena
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/PMC7035424/
https://www.ncbi.nlm.nih.gov/pubmed/32081867
http://dx.doi.org/10.1038/s41598-020-59922-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7035424/
https://www.ncbi.nlm.nih.gov/pubmed/32081867
http://dx.doi.org/10.1038/s41598-020-59922-3

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