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...
Salvato in:
| Autori principali: | Kho, Siew Leng, Chua, Kek Heng, George, Elizabeth, Tan, Mary Anne Jin Ai |
|---|---|
| Natura: | Articolo |
| Lingua: | English |
| Pubblicazione: |
Fundacao de Pesquisas Cientificas de Ribeirao Preto
2013
|
| Accesso online: | http://psasir.upm.edu.my/id/eprint/29670/1/Specific%20and%20straightforward%20molecular%20investigation%20of%20%CE%B2.pdf |
| Tags: |
Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !
|
Documenti analoghi
-
High throughput molecular confirmation of β-thalassemia mutations using novel TaqMan probes
di: Kho, Siew Leng, et al.
Pubblicazione: (2013) -
Molecular characterisation of β-globin gene mutations in Penang and Kedah, Malaysia
di: Kho, Siew Leng, et al.
Pubblicazione: (2014) -
The use of Taqman genotyping assays for rapid confirmation of B-thalassaemia mutations in the Malays: accurate diagnosis with low DNA concentrations
di: Teh, L. K., et al.
Pubblicazione: (2015) -
A TaqMan® multiplex assay for hoofed livestock species identification and nuclear DNA quantification
di: Premasuthan, A., et al.
Pubblicazione: (2017) -
Thalassemia intermedia in HbH-CS disease with compound heterozygosity for β-thalassemia: challenges in hemoglobin analysis and clinical diagnosis
di: Tan, Mary Anne Jin Ai, et al.
Pubblicazione: (2009)
