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Article

Investigating genetic variants in microRNA regulators of Neurokinin-1 receptor in sudden infant death syndrome.

Acta paediatrica (Oslo, Norway : 1992) - 1 Feb 2023

Shaukat Zeeshan, Byard Roger W, Vink Robert, Hussain Rashid, Ricos Michael G, Dibbens Leanne M

Abstract excerpt

Sudden infant death syndrome (SIDS) occurs more often in male than in female infants, suggesting involvement of the X-chromosome. Histopathological studies have suggested that altered expression of the Neurokinin-1 receptor may also play a role in the pathogenesis of SIDS. It was hypothesised that genetic variants in three X-chromosome-encoded microRNA (miRNA/miR), known to down-regulate expression of the...

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Identifiers

PMID: 36271909
DOI: 10.1111/apa.16580
PMCID: PMC10952777

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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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