Gene Mutation Spectrum among Alpha-Thalassaemia Patients in Northeast Peninsular Malaysia

(1) Background: Alpha (α)-thalassaemia is a genetic disorder that affects 5% of the world population. Deletional or nondeletional mutations of one or both HBA1 and HBA2 on chromosome 16 will result in reduced production of α-globin chains, a component of haemoglobin (Hb) that is required for the for...

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Detalles Bibliográficos
Autores principales: Vijian, Divashini, Wan Ab Rahman, Wan Suriana, Ponnuraj, Kannan Thirumulu, Zulkafli, Zefarina, Bahar, Rosnah, Yasin, Norafiza, Hassan, Syahzuwan, Esa, Ezalia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10000533/
https://www.ncbi.nlm.nih.gov/pubmed/36900038
http://dx.doi.org/10.3390/diagnostics13050894

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10000533/
https://www.ncbi.nlm.nih.gov/pubmed/36900038
http://dx.doi.org/10.3390/diagnostics13050894

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