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Article

The genetic and neurobiologic compass points toward common signaling dysfunctions in autism spectrum disorders.

The Journal of clinical investigation - 1 Apr 2009

Levitt Pat, Campbell Daniel B

Abstract excerpt

Autism spectrum disorder (ASD) is a common neurodevelopmental disorder with high heritability. Here, we discuss data supporting the view that there are at least two distinct genetic etiologies for ASD: rare, private (de novo) single gene mutations that may have a large effect in causing ASD; and...

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Identifiers

PMID: 19339766
DOI: 10.1172/JCI37934
PMCID: PMC2662567

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19339766-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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