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Article

Carnitine palmitoyltransferase 2 gene polymorphism is a genetic risk factor for sudden unexpected death in infancy.

Brain & development - 1 Jun 2014

Yamamoto Takuma, Tanaka Hidekazu, Emoto Yuko, Umehara Takahiro, Fukahori Yuki, Kuriu Yukiko, Matoba Ryoji, Ikematsu Kazuya

Abstract excerpt

RATIONALE: Carnitine palmitoyltransferase (CPT) II is one of a pivotal enzyme in mitochondrial fatty acid oxidation, which is essential for energy production during simultaneous glucose sparing and a requirement for major energy supply, such as prolonged fasting or exercise. When infants require...

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Source

Identifiers

PMID: 23969168
DOI: 10.1016/j.braindev.2013.07.011

Genes

CPT2

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-23969168-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

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

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Carnitine palmitoyltransferase 2 gene polymorphism is a genetic risk factor for sudden unexpected death in infancy.PMID 23969168Read ↗

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