Article
Burden of de novo mutations and inherited rare single nucleotide variants in children with sensory processing dysfunction.
BMC medical genomics - 25 May 2018
Marco Elysa Jill, Aitken Anne Brandes, Nair Vishnu Prakas, da Gente Gilberto, Gerdes Molly Rae, Bologlu Leyla, Thomas Sean, Sherr Elliott H
Abstract excerpt
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 with SPD may have pathogenic variants in genes that have been identified as causing other neurodevelopmental...
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