Assessment of B2-Microglobulin Analysis for Renal Insufficiency in Iraqi β-Thalassemia Major Patients

Background: Beta-thalassemia is the most prevalent genetic hemoglobin apathy in the world. It is caused by a reduction or absence of beta-globin chain production, which is typically a portion of adult hemoglobin (HbA, which is α2β2). This genetic anomaly will lead to a rapid erythrocyte turnover, s...

書誌詳細
出版年:	Al-Mustansiriyah Journal of Science
主要な著者:	Estabraq Salman Alwan, Thana Mohammed Juda, Liqaa M. Majed
フォーマット:	論文
言語:	英語
出版事項:	Mustansiriyah University 2024-09-01
主題:	β-thalassemia major B2-microglobulin Ferritin B.Urea Creatinine
オンライン･アクセス:	https://mjs.uomustansiriyah.edu.iq/index.php/MJS/article/view/1391

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