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. 1979 Aug 1;181(2):505–507. doi: 10.1042/bj1810505

Analyis of met-form haemoglobins in human erythrocytes of normal adults and of a patient with hereditary methaemoglobinaemia due to deficiency of NADH-cytochrome b5 reductase.

A Tomoda, M Imoto, M Hirano, Y Yoneyama
PMCID: PMC1161183  PMID: 496898

Abstract

Isoelectric-focusing analysis on an Ampholine/polyacrylamide-gel plate revealed that met-form haemoglobins are present as half-oxidized haemoglobins such as the (alpha 2+ beta 3+)2 and (alpha 3+ beta2+)2 forms rather than as methaemoglobin in the erythrocytes of normal human adults and also of a patient with hereditary methaemoglobinaemia due to deficiency of NADH-cytochrome b5 reductase.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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