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Article

Sudden infant death syndrome: association with a promoter polymorphism of the serotonin transporter gene.

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

Weese-Mayer Debra E, Berry-Kravis Elizabeth M, Maher Brion S, Silvestri Jean M, Curran Mark E, 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, a variable tandem repeat sequence polymorphism in the promoter region of the serotonin transporter protein (5-HTT) gene has recently been associated with risk of SIDS in a Japanese cohort. This polymorphism differentially regulates 5-HTT...

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Identifiers

PMID: 12599191
DOI: 10.1002/ajmg.a.20005

Genes

HTT

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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