Article
Incorporating genotyping to identify patients with G6PD deficiency
2021-02-22
Abstract excerpt
<h4>Background: </h4> Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a common X-linked enzyme disorder associated with hemolytic anemia after exposure to certain medications or foods. Activity testing is the gold standard for detecting G6PD deficiency; however, this test is affected by various hematologic parameters. Clinical G6PD genotyping is included in pharmacogenetic arrays and clinical sequencing and...
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Identifiers and source
- Literature Corpus work
- b264e24c-5be0-56ed-b521-90149a33d72a
- DOI
- 10.22541/au.161403397.70149339/v1
