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Article

SNP association and sequence analysis of the NOS1AP gene in SIDS.

Legal medicine (Tokyo, Japan) - 1 Apr 2009

Osawa Motoki, Kimura Ryousuke, Hasegawa Iwao, Mukasa Nahoko, Satoh Fumiko

Abstract excerpt

One of the speculated causes for sudden infant death syndrome (SIDS) is hereditary disease, in which long QT in electrocardiogram has been investigated in the view of mutations in various ion channel genes. In the present study, a novel QT interval determinant of SNP (rs10494366) in NOS1AP is gen...

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Identifiers

PMID: 19289301
DOI: 10.1016/j.legalmed.2009.01.065

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19289301-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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