An initiation codon mutation ATG-ATA of the p-globin gene was found in seven members of three generations of a family living in northern Sweden. This mutation, which has not previously been described, changes the initiation codon for methionine into a codon for isoleucine and will then result in a p
✦ LIBER ✦
Molecular genetic analyses of β-thalassemia in South India reveals rare mutations in the β-globin gene
✍ Scribed by Murali Dharan Bashyam; Leena Bashyam; Gorinabele R. Savithri; Munimanda Gopikrishna; Vartul Sangal; Akela Radha Rama Devi
- Publisher
- Nature Publishing Group
- Year
- 2004
- Tongue
- English
- Weight
- 260 KB
- Volume
- 49
- Category
- Article
- ISSN
- 1435-232X
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