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Autor:
Ali F.M. El-Sayed, Eman G.E. Helal, Mohammad Abulhasan Zoair, Nahla G. Mohamed, Mona A.M. Ahmed
Publikováno v:
The Egyptian Journal of Hospital Medicine. 57:482-493
Introduction: Thalassemia is a genetic inherited blood disorder in which the body makes abnormal hemoglobin with excessive destruction of red blood cells, which leads to anemia. For many years, hepatitis B virus was a major problem for patients with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a090583c29f725e58347febe5396e4d8
https://doi.org/10.12816/0008483
https://doi.org/10.12816/0008483
