Answers are grounded in this paper and cite their sources.
Summary 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.
No takes yet. Share an insight, caveat, or question.
Stephens et al. (2011) studied this question.
Synapse has enriched 5 related papers. Consider them for comparative context: