The effect of HBB: c.*+96T>C (3'UTR +1570 T>C) on the mild b-thalassemia intermedia phenotype
Hemoglobin beta (HBB): c.*+96T>C substitution is very rare among β-globin gene mutations and its clinical significance remains to be clarified. The present study aimed to investigate the role of HBB: c.*+96T>C in the β-thalassemia intermedia phenotype in a Turkish family. The proband and...
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| Hoofdauteurs: | , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Turkish Society of Hematology
2011-08-01
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| Reeks: | Turkish Journal of Hematology |
| Onderwerpen: | |
| Online toegang: | https://jag.journalagent.com/z4/download_fulltext.asp?pdir=tjh&un=TJH-48742 |
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