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London family welcomes research findings into a rare inherited type of anaemia
13-year-old Robi was diagnosed with congenital dyserythropoietic anaemia type 1 (CDA-1) aged nine months and has needed blood transfusions and interferon injections his whole life.
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Meet the researcher: Dr Eva Ioannidou
Dr Ioannidou is an Action Medical Research and British Paediatric Neurology Association Research Training Fellow.
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