Detection of hemoglobin Kinshasa by a capillary electrophoresis method.
(2022) Clinica Chimica Acta — Vol. 531, p. 81-83 (2022)
Files
2022_Deltombe_Clin_Chim_Acta_Ab.pdf
Abstract Scopus
Open Access - Adobe PDF
- 81.59 KB
2022_Deltombe_Clin_Chim_Acta.pdf
Restricted Access - Adobe PDF
- 905.97 KB
Details
- Authors
- Abstract
- INTRODUCTION: Hemoglobinopathies are autosomal recessive disorders. Among them, α-Thalassemia (α-thal), a disorder induced most of the time by deletions of α genes on chromosome 16, and more rarely by a mutation (nondeletional α-thal), is characterized by a microcytic hypochromic anemia. [...]
- Affiliations
Citations
Deltombe, M., Benamour, M., Derclaye, I., & Maisin, D. (2022). Detection of hemoglobin Kinshasa by a capillary electrophoresis method. Clinica Chimica Acta, 531, 81-83. https://doi.org/10.1016/j.cca.2022.03.020 (Original work published 2022)