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Article

Noncardiac genetic predisposition in sudden infant death syndrome.

Genetics in medicine : official journal of the American College of Medical Genetics - 1 Mar 2019

Gray Belinda, Tester David J, Wong Leonie Ch, Chanana Pritha, Jaye Amie, Evans Jared M, Baruteau Alban-Elouen, Evans Margaret, Fleming Peter, Jeffrey Iona, Cohen Marta, Tfelt-Hansen Jacob, Simpson Michael A, Ackerman Michael J, Behr Elijah R

Abstract excerpt

PURPOSE: Sudden infant death syndrome (SIDS) is the commonest cause of sudden death of an infant; however, the genetic basis remains poorly understood. We aimed to identify noncardiac genes underpinning SIDS and determine their prevalence compared with ethnically matched controls. METHODS: Using exome sequencing we assessed the yield of ultrarare nonsynonymous variants (minor allele frequency [MAF] ≤0.00005,...

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Identifiers

PMID: 30139991
DOI: 10.1038/s41436-018-0131-4

Genes

MAF
ECE1

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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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