Simple method for screening of α-thalassaemia 1 carriers
α-Thalassaemia 1 genetic disorder occurs when there is a deletion of two linked α-globin genes. The interaction between these abnormal genes leads to the most severe type of thalassaemia disease, haemoglobin (Hb) Bart's hydrops fetalis. The identification of α-thalassaemia 1 carriers and geneti...
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| Main Authors: | , , , , , , , |
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| 格式: | 雜誌 |
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2018
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| 在線閱讀: | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=67749088035&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/59833 |
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| 機構: | Chiang Mai University |