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[Of these 2637 cases, 705 (26.7%) carried ?(+)-thalassemia with eight different mutations including 6 promoter mutations; NT-28 (A-G), NT-31 (A-G), NT-50 (G-A), NT-86 (C-G), NT-87 (C-A) and NT-90 (C-T) and two missense mutations; Hb Malay (codon 19; AAC-AGC) and Hb Dhonburi (codon 126; GTG-GGG).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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