Llwytho...
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...
Wedi'i Gadw mewn:
| Prif Awduron: | , , , , , , , , , , |
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| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
American Society of Hematology
2009
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| Pynciau: | |
| Mynediad Ar-lein: | 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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