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Amelioration of Sardinian β(0) thalassemia by genetic modifiers
Sardinian β-thalassemia patients all are homozygotes for the same null allele in the β-globin gene, but the clinical manifestations are extremely variable in severity. Previous studies have shown that the coinheritance of α-thalassemia or the presence of genetic variants that sustain fetal hemoglobi...
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| 主要な著者: | , , , , , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
American Society of Hematology
2009
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2925722/ https://ncbi.nlm.nih.gov/pubmed/19696200 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2009-04-217901 |
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