Abstract:
: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.
journal_name
Hum Genetjournal_title
Human geneticsauthors
Winichagoon P,Kownkon J,Yenchitsomanus P,Thonglairoam V,Siritanaratkul N,Fucharoen Sdoi
10.1007/BF00274004subject
Has Abstractpub_date
1989-07-01 00:00:00pages
389-90issue
4eissn
0340-6717issn
1432-1203journal_volume
82pub_type
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