Mild thalassemia: the result of interactions of alpha and beta thalassemia genes
Homozygous thalassemia is due to inherited unbalanced synthesis of the α- or β-chains of hemoglobin. Clinical severity may be in part related to the extent of α:β imbalance. Two families are presented that illustrate this concept. Thalassemia in these individuals was evaluated by clinical and geneti...
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| Udgivet i: | J Clin Invest |
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| Principais autores: | , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
American Society for Clinical Investigation
1970
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC322517/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/5443168/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI106274 |
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