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What is Alfa Talasemi ve MLPA Analizi about?

This study investigates the molecular characterization of alpha thalassemia in 29 patients in Konya, Turkey, using Multiplex Ligation Dependent Probe Amplification (MLPA) to analyze alpha globin gene variations. Results showed that 51.7% of patients had deletions, with the most common being -α 3.7, and the study emphasizes the importance of MLPA in diagnosing alpha thalassemia. The findings suggest that further sequencing of HBA1 and HBA2 genes may be necessary in cases where MLPA results do not explain the

Author

fatmabykoglan76

Language

EN