During a physical checkup, a 42-year-old Japanese man with liver dysfunction was diagnosed as having p-thalassemia. Using molecular biological techniques including PCR, we investigated the chemical basis of the hematological disorder. We found that a frameshift attributable to the insertion of a thy
✦ LIBER ✦
β0-Thalassemia resulting from a novel mutation: β66/u→stop codon
✍ Scribed by C.R.E. Grignoli; M.H. Carvalho; E.M. Kimura; M.F. Sonati; V.R. Arruda; S.T.O. Saad; F.F. Costa
- Book ID
- 114422938
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 65 KB
- Volume
- 64
- Category
- Article
- ISSN
- 0902-4441
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