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Diagnosis of Compound Heterozygous Hb Tak/β-Thalassemia and HbD-Punjab/β-Thalassemia by HbA(2) Levels on Capillary Electrophoresis
A misdiagnosis of β-thalassemia carrier in samples with Hb Tak and HbD-Punjab, the β-variants, can be a cause of inappropriate genetic counseling thus having a new case of β-thalassemia major. A capillary electrophoresis (CE) is very efficient in separating and quantifying HbA(2). In this study, HbA...
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| Izdano u: | Indian J Hematol Blood Transfus |
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| Glavni autori: | , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Springer India
2017
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5786607/ https://ncbi.nlm.nih.gov/pubmed/29398808 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12288-017-0810-3 |
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