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Modification of Hemoglobin H Disease by Sickle Trait
The rarity of hemoglobin (Hb) H disease in combination with sickle trait may be due in part to the absence of actual Hb H in individuals who, nonetheless, have inherited the deletion of three α-globin genes. We describe here a boy with persistent microcytic, hypochromic anemia despite adequate iron...
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| Hlavní autoři: | , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
1979
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC372212/ https://ncbi.nlm.nih.gov/pubmed/479366 |
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