Zobrazeno 1 - 1
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pro vyhledávání: '"Madyan Mohammed Fawzi Al-Ghrer"'
Publikováno v:
Romanian Journal of Pharmaceutical Practice, Vol 16, Iss 3-4, Pp 52-56 (2023)
Background. Thalassemia is congenital disease case by mutation effect to synthesis of beta globin chain of hemoglobin result in combination of metabolic and endocrine disorder. Bone disease is a not rare complication in thalassemia due to malabsorpti
Externí odkaz:
https://doaj.org/article/a72e4dc4c92344b5994c616e980afb20
