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Prevalence of 3.7 and 4.2 deletions in Sudanese patients with red cells hypochromia and microcytosis
OBJECTIVE: Alpha-thalassemia is a genetic disorder characterized by deletions of one or more α globin genes that result in deficient of α globin chains reducing haemoglobin concentration. The study aimed to screen 97 patients with microcytosis and hypochromasia for the 3.7 and 4.2 alpha thalassemia...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7011266/ https://www.ncbi.nlm.nih.gov/pubmed/32041645 http://dx.doi.org/10.1186/s13104-020-4933-5 |