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...
Uloženo v:
| Hlavní autoři: | Kho, Siew Leng, Chua, Kek Heng, George, Elizabeth, Tan, Mary Anne Jin Ai |
|---|---|
| Médium: | Článek |
| Jazyk: | English |
| Vydáno: |
Fundacao de Pesquisas Cientificas de Ribeirao Preto
2013
|
| On-line přístup: | http://psasir.upm.edu.my/id/eprint/29670/1/Specific%20and%20straightforward%20molecular%20investigation%20of%20%CE%B2.pdf |
| Tagy: |
Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!
|
Podobné jednotky
-
High throughput molecular confirmation of β-thalassemia mutations using novel TaqMan probes
Autor: Kho, Siew Leng, a další
Vydáno: (2013) -
Molecular characterisation of β-globin gene mutations in Penang and Kedah, Malaysia
Autor: Kho, Siew Leng, a další
Vydáno: (2014) -
The use of Taqman genotyping assays for rapid confirmation of B-thalassaemia mutations in the Malays: accurate diagnosis with low DNA concentrations
Autor: Teh, L. K., a další
Vydáno: (2015) -
A TaqMan® multiplex assay for hoofed livestock species identification and nuclear DNA quantification
Autor: Premasuthan, A., a další
Vydáno: (2017) -
Thalassemia intermedia in HbH-CS disease with compound heterozygosity for β-thalassemia: challenges in hemoglobin analysis and clinical diagnosis
Autor: Tan, Mary Anne Jin Ai, a další
Vydáno: (2009)
