Reasons of Unknown HPLC Peaks during Hemoglobin Analysis for Patients with Beta Thalassemias
Beta-thalassemias (β-thal) are inherited quantitative disorders of haemoglobin (Hb) leading to underproduction of the beta globin chains of hemoglobin. In β-thal, the synthesis of normal α globin chains from the unaffected α globin gene continues as normal, resulting in the accumulation within the e...
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| Main Authors: | , |
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| Format: | Article |
| Language: | English |
| Published: |
2014
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| Subjects: | |
| Online Access: | http://eprints.unisza.edu.my/4757/1/FH02-FP-15-02863.pdf http://eprints.unisza.edu.my/4757/ http://esciencecentral.org/journals/reasons-of-unknown-hplc- |
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