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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Bibliographic Details
Main Authors: Chatchai Tayapiwatana, Surakit Kuntaruk, Thanusak Tatu, Sawitree Chiampanichayakul, Thongperm Munkongdee, Pranee Winichagoon, Suthat Fuchareon, Watchara Kasinrerk
Format: Journal
Published: 2018
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Online Access: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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Institution: Chiang Mai University
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