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Cited by 430

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Glucose-6-Phosphate Dehydrogenase Deficiency

Desforges, Jane F., Beutler, Ernest·1991·New England Journal of Medicine

Abstract

IT has been estimated that the red cells of more than 200 million people are deficient in the enzyme glucose-6-phosphate dehydrogenase (G6PD). This X-linked hereditary deficiency was discovered more than 30 years ago as an outgrowth of studies of the unique sensitivity of some persons to the hemolytic action of drugs.1 Since that time much has been learned about the population genetics of G6PD deficiency and its effect on human health. More than 400 putative variants of the enzyme have been described, distinguished by their biochemical characteristics. However, some once-accepted concepts concerning the relation between G6PD deficiency and hemolysis have . . .

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Metadata

Authors
Desforges, J. F., & Beutler, E.
Venue
New England Journal of Medicine
Published
1991-01-17
Volume
324
Issue
3
Pages
169-174
ISSN
  • 0028-4793 (ISSN-L)
  • 1533-4406
OpenAlex
W1991042120
Cited by
430
References
1
FWCI
40.02
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Glucose-6-Phosphate Dehydrogenase Deficiency. https://app.cochat.ai/papers/10.1056/nejm199101173240306
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Desforges, J. F., & Beutler, E. (1991). Glucose-6-Phosphate Dehydrogenase Deficiency. New England Journal of Medicine. https://doi.org/10.1056/nejm199101173240306

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.