Burden of de novo mutations and inherited rare single nucleotide variants in children with sensory processing dysfunction

BACKGROUND: In children with sensory processing dysfunction (SPD), who do not meet criteria for autism spectrum disorder (ASD) or intellectual disability, the contribution of de novo pathogenic mutation in neurodevelopmental genes is unknown and in need of investigation. We hypothesize that children...

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Detalles Bibliográficos
Autores principales: Marco, Elysa Jill, Aitken, Anne Brandes, Nair, Vishnu Prakas, da Gente, Gilberto, Gerdes, Molly Rae, Bologlu, Leyla, Thomas, Sean, Sherr, Elliott H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5970458/
https://www.ncbi.nlm.nih.gov/pubmed/29801487
http://dx.doi.org/10.1186/s12920-018-0362-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5970458/
https://www.ncbi.nlm.nih.gov/pubmed/29801487
http://dx.doi.org/10.1186/s12920-018-0362-x

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