Multiplex Minisequencing of the HBB Gene: A Rapid Strategy to Confirm the Most Frequent β-Thalassemia Mutations in the Tunisian Population. [electronic resource]
- Hemoglobin 2015
- 251-5 p. digital
Publication Type: Journal Article
1532-432X
10.3109/03630269.2015.1041605 doi
Genotype Humans Mutation Phenotype Sequence Analysis, DNA Tunisia--epidemiology beta-Globins--genetics beta-Thalassemia--epidemiology