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Article

Mutation screening of X-chromosomal neuroligin genes: no mutations in 196 autism probands.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics - 15 Aug 2004

Vincent John B, Kolozsvari Debbie, Roberts Wendy S, Bolton Patrick F, Gurling Hugh M D, Scherer Stephen W

Abstract excerpt

Autism, a childhood neuropsychiatric disorder with a strong genetic component, is currently the focus of considerable attention within the field of human genetics as well many other medical-related disciplines. A recent study has implicated two X-chromosomal neuroligin genes, NLGN3 and NLGN4, as having an etiological role in autism, having identified a frameshift mutation in one gene and a substitution mutation...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 15274046
DOI: 10.1002/ajmg.b.30069

Genes

NLGN3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Mutation screening of X-chromosomal neuroligin genes: no mutations in 196 autism probands.PMID 15274046Read ↗

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