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Article

A functional polymorphism in the tyrosine hydroxylase gene indicates a role of noradrenalinergic signaling in sudden infant death syndrome.

The Journal of pediatrics - 1 Aug 2008

Klintschar Michael, Reichenpfader Barbara, Saternus Klaus-Steffen

Abstract excerpt

OBJECTIVES: Catecholamines may contribute to the cause of sudden infant death syndrome (SIDS). TH01, a tetrameric short tandem repeat marker in the tyrosine hydroxylase gene, regulates gene expression and catecholamine production. STUDY DESIGN: We investigated TH01 in 172 German Caucasian SIDS ca...

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Source

Identifiers

PMID: 18534229
DOI: 10.1016/j.jpeds.2008.02.032

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-18534229-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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