Article
The spectrum of beta-thalassemia mutations in the Oran region of Algeria.
Hemoglobin - 1 May 1994
Bouhass R, Perrin P, Trabuchet G
Abstract excerpt
In order to delineate the spectrum of beta-globin gene defects causing beta-thalassemia in the Oran region of Algeria, we have analyzed a representative sample of 31 beta-thalassemia patients. This led to the detection of 10 mutations. Four of them [nonsense codon 39 (C->T), IVS-I-110 (G->A), IVS...
Topics
- Adult
- Algeria
- Base Sequence
- Codon
- Frameshift Mutation
- Genetic Variation
- Heterozygote
- Homozygote
- Humans
- Male
- Molecular Sequence Data
- Mutation
- beta-Thalassemia
