The use of Taqman genotyping assays for rapid confirmation of B-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...
محفوظ في:
| المؤلفون الرئيسيون: | , , , , |
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| التنسيق: | مقال |
| اللغة: | English |
| منشور في: |
Wiley-Blackwell Publishing
2015
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| الوصول للمادة أونلاين: | http://psasir.upm.edu.my/id/eprint/46713/1/The%20use%20of%20Taqman%20genotyping%20assays%20for%20rapid%20confirmation%20of%20B-thalassaemia%20mutations%20in%20the%20Malays%3B%20accurate%20diagnosis%20with%20low%20DNA%20concentrations_New.pdf |
| الوسوم: |
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