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Hemoglobin A (HbA), also known as adult hemoglobin, hemoglobin A1 or α2β2, is the most common human hemoglobin tetramer, accounting for over 97% of the total red blood cell hemoglobin. Hemoglobin is an oxygen-binding protein, found in erythrocytes, which transports oxygen from the lungs to the tissues. Hemoglobin A is the most common adult form of…
Clinical significance, Synthesis & Structure and function
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hemoglobin cell sickle alpha oxygen common form two heme due blood subunits hb chain beta adult synthesis gene red globin
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| Hemoglobin A | is a | most common adult form of hemoglobin and exists as a tetramer containing two alpha subunits and two beta subunits | 0.90 | text |
| mutations or deletions in genes coding for the globin chain can occur | instance of | Heme synthesis involves multiple enzymes and when these enzymes are deficient or do not function properly consequences | 0.80 | text |
| Hemoglobin A | related to Sickle cell disease | Sickle | 0.60 | section |
| Hemoglobin A | related to Sickle cell disease | HbS | 0.60 | section |
| Hemoglobin A | related to Sickle cell disease | There | 0.60 | section |
| Hemoglobin A | related to Sickle cell disease | HB SS | 0.60 | section |
| Hemoglobin A | related to Sickle cell disease | Hb SC | 0.60 | section |
| Hemoglobin A | related to Sickle cell disease | Hb | 0.60 | section |
| Hemoglobin A | related to Sickle cell disease | In | 0.60 | section |
| Hemoglobin A | related to Sickle cell disease | HbAS | 0.60 | section |
| Hemoglobin A | related to Sickle cell disease | HbA | 0.60 | section |
| Hemoglobin A | related to Sickle cell disease | This | 0.60 | section |
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