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Article

Genetic variation in hepatic glucose-6-phosphatase system genes in cases of sudden infant death syndrome.

The Journal of pathology - 1 May 2007

Forsyth L, Scott H M, Howatson A, Busuttil A, Hume R, Burchell A

Abstract excerpt

Genetic deficiencies of the hepatic glucose-6-phosphatase system, either of the enzyme (G6PC1) or of the glucose-6-phosphate transporter (G6PT1), result in fasting hypoglycaemia. Low hepatic G6PC1 activities were previously reported in a few term sudden infant death syndrome (SIDS) infants and assumed to be due to G6PC1 genetic deficiencies. In preterm infants, failures of postnatal activation of G6PC1 expression...

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Identifiers

PMID: 17354259
DOI: 10.1002/path.2147

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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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