Identification of molecular basis of [beta]-thalassemia/HbE gene in Thai population using synthetic oligonucleotide probes

β-Thalassemia is a genetic disorder causing a complete absence of B-globin chain in hemoglobin. In Thai population, β-Thalassemia associated with HbE (β(26)GAG--->AAG) is found in high frequency. More than 50 types of molecular mutations in B-thalassemic gene have been reported, including large s...

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Bibliographic Details
Main Author: Songsak Petmitr
Other Authors: Prapon Wilairat
Language:English
Published: Mahidol University. Mahidol University Library and Knowledge Center 2023
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/89664
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Institution: Mahidol University
Language: English