HBB Gene Mutations and Their Pathological Impacts on HbE/β-Thalassaemia in Kuala Terengganu, Malaysia

Background: β-thalassaemia is a disorder caused by mutations in the β-globin gene, leading to defective production of haemoglobins (Hb) and red blood cells (RBCs). It is characterised by anaemia, ineffective erythropoiesis, and iron overload. Patients with severe β-thalassaemia require lifelong bloo...

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Detalles Bibliográficos
Autores principales: Saad, Hanan Kamel M., Taib, Wan Rohani Wan, Ab Ghani, Azly Sumanty, Ismail, Imilia, Al-Rawashde, Futoon Abedrabbu, Almajali, Belal, Alhawamdeh, Maysa, Abd Rahman, Alawiyah Awang, Al-wajeeh, Abdullah Saleh, Al-Jamal, Hamid Ali Nagi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10147086/
https://www.ncbi.nlm.nih.gov/pubmed/37046464
http://dx.doi.org/10.3390/diagnostics13071247

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10147086/
https://www.ncbi.nlm.nih.gov/pubmed/37046464
http://dx.doi.org/10.3390/diagnostics13071247

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