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Turk J Med Sci ; 47(3): 973-978, 2017 Jun 12.
Article in English | MEDLINE | ID: mdl-28618753

ABSTRACT

BACKGROUND/AIM: IVSI-110 (G>A), IVSI-6 (T>C), IVSII-1 (G>A), IVSII-745 (C>G), IVSI-1 (G>A), and HbS are mutations covering 76% of all the ß-globin mutations in the Turkish population. In this study, our aim is to develop a reliable, fast, real-time kit for these mutations using the TaqMan probe method. MATERIALS AND METHODS: This study included 100 individuals with beta-thalassemia or sickle cell anemia who had unknown mutations, and 21 controls with known mutations. RESULTS: We designed a kit containing the IVSI-110 (G>A), IVSI-6 (T>C), IVSII-1 (G>A), IVSII-745 (C>G), IVSI-1 (G>A), and HbS mutations by using the real-time PCR method. One hundred patients were studied with our developed TaqMan real-time PCR kit. Of these patients, 73 (73%) were identified with the beta gene mutation. Among those 73 patients, 16 were homozygous, 54 were heterozygous, and 3 were compound heterozygous. CONCLUSION: This reliable kit provided rapid diagnosis including 76% of the ß-thalassemia mutations in Turkey.


Subject(s)
Hemoglobin, Sickle/genetics , Mutation/genetics , Real-Time Polymerase Chain Reaction/methods , beta-Thalassemia , DNA Mutational Analysis/methods , Humans , Reproducibility of Results , Turkey , beta-Thalassemia/diagnosis , beta-Thalassemia/genetics
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