Compound Heterozygosity for Hb Hope and β⁰-thalassaemia (codon 41/42 −TTCC) in a Myanmar Girl: A Rare Cause of Non-transfusion-dependent Thalassaemia (NTDT)
Fields of Study & Subjects
Hemoglobinopathies and Related Disorders
Iron Metabolism and Disorders
Blood groups and transfusion
Publication details
- Publication date
- 1 January 2026
- Language
- ID