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

• Main Authors: Elysa Jill Marco (Author), Anne Brandes Aitken (Author), Vishnu Prakas Nair (Author), Gilberto da Gente (Author), Molly Rae Gerdes (Author), Leyla Bologlu (Author), Sean Thomas (Author), Elliott H. Sherr (Author)
• Format: Book
• Published: BMC, 2018-05-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Abstract 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...