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...

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Detalles Bibliográficos
Autores principales: Osman, Hussam Ali, Hamid, Muzamil Mahdi Abdel, Ahmad, Rahimah Binti, Saleem, Mohamed, Abdallah, Sana Altahir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research Note
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

Internet

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

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