Burden of de novo mutations and inherited rare single nucleotide variants in children with sensory processing dysfunction
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...
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| Main Authors: | , , , , , , , |
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| Format: | Book |
| Published: |
BMC,
2018-05-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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