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  1. Fulltext Molecular identification of a rare haemoglobin variant: Hb G coushatta in Malaysia
    Alifah Nadia Abu Hassan, Ezalia Esa, Nur Aisyah Aziz, Faidatul Syazlin Abd Hamid, Zubaidah Zakaria, Siti Aisyah Lazim
    Journal of Biomedical and Clinical Sciences, 2017;2(202):1-2.
    MyJurnal
    Thalassaemia screening programme was conducted to reduce the burden of the disease [1]. Here, we describe one unexpected discovery in a 33-year-old gentleman and also the importance of DNA analysis in detecting the globin gene mutation.
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