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Article

PCR-based allelic discrimination for glucose-6-phosphate dehydrogenase (G6PD) deficiency in Ugandan umbilical cord blood.

Pediatric hematology and oncology - 1 Feb 2014

Hsu Jennifer, Fink Deanna, Langer Erica, Carter Michelle L, Bengo Derrik, Ndidde Susan, Slusher Tina, Ross Julie A, Lund Troy C

Abstract excerpt

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common X-linked disorder in the world. G6PD deficiency puts children at risk for hyperbilirubinemia and kernicterus during the newborn period and an increased risk of severe hemolysis after exposure to many antimalarial medications. A laboratory diagnosis of G6PD deficiency is rare in the developing world due to limited resources. We developed a...

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Identifiers

PMID: 24308819
DOI: 10.3109/08880018.2013.860649
PMCID: PMC3923300

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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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