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pro vyhledávání: '"Mohammed Mahmoud Hassan Omar"'
Autor:
Mervat Abdallah Hesham, Usama Roshdy El-Safy, Yosria Abd-Hameed El-Taweel, Mohammed Mahmoud Hassan Omar
Publikováno v:
Egyptian Journal of Hospital Medicine; Vol. 86 No. 1 (2022); 391-397
Background: Beta thalassemia syndrome is a hereditary disorder characterized by reduced or absent synthesis of thebeta chains of hemoglobin that disturbs the normal shape of red blood cells. Chronic hypoxia of the nerves resulting from severe anemia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77c4fbf7630520f2eef59019b8f40c0d
https://www.ajol.info/index.php/ejhm/article/view/223591
https://www.ajol.info/index.php/ejhm/article/view/223591
