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Article

Possible association of 3' UTR +357 A>G, IVS11-nt 93 T>C, c.1311 C>T polymorphism with G6PD deficiency.

Hematology (Amsterdam, Netherlands) - 1 Jul 2017

Sirdah Mahmoud M, Shubair Mohammad E, Al-Kahlout Mustafa S, Al-Tayeb Jamal M, Prchal Josef T, Reading N Scott

Abstract excerpt

BACKGROUND: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a common X-linked inherited enzymopathic disorder affecting more than 500 million people worldwide. It has so far been linked to 217 distinct genetic variants in the exons and exon-intron boundaries of the G6PD gene, giving rise to a wide range of biochemical heterogeneity and clinical manifestations. OBJECTIVES: Reports from different settings...

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Identifiers

PMID: 28059001
DOI: 10.1080/10245332.2016.1276117

Variants

rs2071429

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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