Impact of genotype on endocrinal complications in β-thalassemia patients

In β-thalassemia, certain mutations cause a complete absence of β-globin chain synthesis, termed β(0)-thalassemia, while others may allow certain β-globin production and are termed β(+)- or β(++)-thalassemia. The homozygous state results in severe anemia, which requires regular blood transfusion. By...

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Udgivet i:Biomed Rep
Main Authors: AL-AKHRAS, AHMED, BADR, MOHAMED, EL-SAFY, USAMA, KOHNE, ELISABETH, HASSAN, TAMER, ABDELRAHMAN, HADEEL, MOURAD, MOHAMED, BRINTRUP, JOAQUIN, ZAKARIA, MARWA
Format: Artigo
Sprog:Inglês
Udgivet: D.A. Spandidos 2016
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Articles
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4887852/
https://ncbi.nlm.nih.gov/pubmed/27284414
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/br.2016.646
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