Article
C-->T mutation at -158 G gamma HPFH associated with 4 bp deletion (-225-222) in the promoter region of the A gamma gene in homozygous beta 0 39 nonsense thalassemia.
Haematologica - 1 Jan 1999
Ataulfo Gonzalez F, Ropero P, Sánchez J, Rosatellí C, Galanello R, Villegas A
Abstract excerpt
No abstract is available from the source.
Topics
- Adult
- Codon
- Female
- Fetal Hemoglobin
- Gene Expression Regulation, Developmental
- Globins
- Haplotypes
- Homozygote
- Humans
- Male
- Phenotype
- Point Mutation
- Promoter Regions, Genetic
- Sequence Deletion
- beta-Thalassemia
