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Detection of β-thalassemia and hemoglobin E genes in Thai by a DNA amplification technique

✍ Scribed by Pranee Winichagoon; Jiraporn Kownkon; Pathai Yenchitsomanus; Varaporn Thonglairoam; Nopadol Siritanaratkul; Suthat Fucharoen


Publisher
Springer
Year
1989
Tongue
English
Weight
222 KB
Volume
82
Category
Article
ISSN
0340-6717

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✦ Synopsis


Enzymatic DNA amplification and polyacrylamide gel electrophoresis, which demonstrate different sizes of DNA fragments, were used to detect the common mutations causing beta-thalassemia and hemoglobin (Hb) E in Thai people. The 4-bp deletion at codons 41 and 42 can be detected directly by polyacrylamide gel electrophoresis and ethidium bromide staining. Whereas the nonsense mutations at codon 17 (AAG----TAG) and Hb E (GAG----AAG at codon 26) were detected after digestion of the amplified DNA with the enzymes MaeI and MnlI, respectively.


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