Title : Is hemoglobin instability important in the interaction between hemoglobin E and beta thalassemia?

Pub. Date : 1998 Sep 15

PMID : 9731073






2 Functional Relationships(s)
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Sentence
Compound Name
Protein Name
Organism
1 Hemoglobin E (HbE; alpha2beta226glu-lys), globally the commonest hemoglobin variant, is synthesized at a slightly reduced rate and has a homozygous phenotype similar to heterozygous beta thalassemia. alpha2beta226glu hemoglobin subunit epsilon 1 Homo sapiens
2 Hemoglobin E (HbE; alpha2beta226glu-lys), globally the commonest hemoglobin variant, is synthesized at a slightly reduced rate and has a homozygous phenotype similar to heterozygous beta thalassemia. Lysine hemoglobin subunit epsilon 1 Homo sapiens