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Spectrum of Genetic Mutation in Beta Globin Gene in Various Type of Thalassaemia in Bangladesh

Background: Hb-E/Beta thalassaemia is a congenital haemoglobin disorder which is a compound heterozygous state consists of qualitative disorder like Hb E variant & quantitative Hb disorder caused by genetic mutation of Beta chain. Objective: The aim of the study was to identify the beta gene mutati...

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Principais autores: Nishat Mahzabin, Md. Akhlak-Ul- Islam, Kazi Mohammad Kamrul Islam, Khaza Amirul Islam, Md. Arif-Ur- Rahman, Nusrat Jahan, Amin Lutful Kabir
Format: Artigo
Sprog:Inglês
Udgivet: Haematology Society of Bangladesh 2021-11-01
Serier:Haematology Journal of Bangladesh
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Online adgang:https://journal.hematologybd.org/index.php/haematoljbd/article/view/77
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