The use of Taqman genotyping assays for rapid confirmation of β-thalassaemia mutations in the Malays: accurate diagnosis with low DNA concentrations
Introduction: In Malaysia, β-thalassaemia is a common inherited blood disorder in haemoglobin synthesis with a carrier rate of 4.5%. Currently, PCR-incorporating techniques such as amplification refractory mutation system (ARMS) or reverse dot blot hybridization (RDBH) are used in β-thalassaemia mut...
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| Main Authors: | , , , , |
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| Format: | Article |
| Published: |
Wiley
2014
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| Subjects: | |
| Online Access: | http://eprints.um.edu.my/19575/ http://dx.doi.org/10.1111/ijlh.12240 |
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