A Novel Frameshift Mutation at Codons 138/139 (HBB: c.417_418insT) on the β-Globin Gene Leads to β-Thalassemia. [electronic resource]
- Hemoglobin Jan 2017
- 59-60 p. digital
Publication Type: Case Reports; Journal Article
1532-432X
10.1080/03630269.2017.1295986 doi
Adult Alleles Amino Acid Substitution Codon DNA Mutational Analysis Erythrocyte Indices Exons Frameshift Mutation Genetic Association Studies Heterozygote Humans Male Phenotype beta-Globins--genetics beta-Thalassemia--blood