Abstract
Although DNA analysis is needed for characterization of the mutations that cause β-thalassaemia, measurement of the Hb A 2 is essential for the routine identification of people who are carriers of β-thalassaemia. The methods of quantitating Hb A 2 are described together with pitfalls in undertaking these laboratory tests with particular emphasis on automated high-performance liquid chromatography and capillary electrophoresis.
Original language | English (US) |
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Pages (from-to) | 1-13 |
Number of pages | 13 |
Journal | International Journal of Laboratory Hematology |
Volume | 34 |
Issue number | 1 |
DOIs | |
State | Published - Feb 2012 |
Keywords
- Capillary electrophoresis
- HPLC
- Haemoglobinopathy
- Hb A
- Recommended methods
- Thalassaemia
ASJC Scopus subject areas
- Hematology
- Clinical Biochemistry
- Biochemistry, medical