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Article

Association of the serotonin transporter gene with sudden infant death syndrome: a haplotype analysis.

American journal of medical genetics. Part A - 15 Oct 2003

Weese-Mayer Debra E, Zhou Lili, Berry-Kravis Elizabeth M, Maher Brion S, Silvestri Jean M, Marazita Mary L

Abstract excerpt

Serotonergic receptor binding in the arcuate nucleus, n. raphé obscurus, and other medullary regions is decreased in sudden infant death syndrome (SIDS) cases. Further, an insertion/deletion polymorphism in the promoter region of the serotonin transporter protein (5-HTT) gene has recently been as...

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Source

Identifiers

PMID: 12966525
DOI: 10.1002/ajmg.a.20427

Genes

HTT

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-12966525-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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