Specific and straightforward molecular investigation of β-thalassemia mutations in the Malaysian Malays and Chinese using direct TaqMan genotyping assays
Beta-thalassemia is a life-threatening inherited blood disorder. Rapid characterization of β-globin gene mutations is necessary because of the high frequency of Malaysian β-thalassemia carriers. A combination real-time polymerase chain reaction genotyping assay using TaqMan probes was developed to c...
محفوظ في:
| المؤلفون الرئيسيون: | Kho, Siew Leng, Chua, Kek Heng, George, Elizabeth, Tan, Mary Anne Jin Ai |
|---|---|
| التنسيق: | مقال |
| اللغة: | English |
| منشور في: |
Fundacao de Pesquisas Cientificas de Ribeirao Preto
2013
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| الوصول للمادة أونلاين: | http://psasir.upm.edu.my/id/eprint/29670/1/Specific%20and%20straightforward%20molecular%20investigation%20of%20%CE%B2.pdf |
| الوسوم: |
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مواد مشابهة
-
High throughput molecular confirmation of β-thalassemia mutations using novel TaqMan probes
بواسطة: Kho, Siew Leng, وآخرون
منشور في: (2013) -
Molecular characterisation of β-globin gene mutations in Penang and Kedah, Malaysia
بواسطة: Kho, Siew Leng, وآخرون
منشور في: (2014) -
The use of Taqman genotyping assays for rapid confirmation of B-thalassaemia mutations in the Malays: accurate diagnosis with low DNA concentrations
بواسطة: Teh, L. K., وآخرون
منشور في: (2015) -
A TaqMan® multiplex assay for hoofed livestock species identification and nuclear DNA quantification
بواسطة: Premasuthan, A., وآخرون
منشور في: (2017) -
Thalassemia intermedia in HbH-CS disease with compound heterozygosity for β-thalassemia: challenges in hemoglobin analysis and clinical diagnosis
بواسطة: Tan, Mary Anne Jin Ai, وآخرون
منشور في: (2009)
