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Article

Reelin gene alleles and susceptibility to autism spectrum disorders.

Molecular psychiatry - 1 Jan 2002

Zhang H, Liu X, Zhang C, Mundo E, Macciardi F, Grayson D R, Guidotti A R, Holden J J A

Abstract excerpt

A polymorphic trinucleotide repeat (CGG/GCC) within the human Reelin gene (RELN) was examined as a candidate gene for autism spectrum disorders (ASDs). This gene encodes a large extracellular matrix protein that orchestrates neuronal positioning during corticogenesis. The CGG-repeat within the 5' untranslated region of RELN exon 1 was examined in 126 multiple-incidence families. The number of CGG repeats varied...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 12399956
DOI: 10.1038/sj.mp.4001124

Genes

RELN

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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