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PDF Availablehttps://doi.org/10.1136/jmedgenet-2020-106880
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Cite Journal: Journal of medical genetics |  Publication Date: Jun 9, 2020 |
 Citations: 13 |  License type: other-oa |
Affiliation: University of Oxford, MRC Weatherall Institute of Molecular Medicine, Uppsala University, Uppsala University Hospital, Oxford University Hospitals NHS Trust, John Radcliffe Hospital, Oxford BioMedica (United Kingdom), Novo Nordisk (Denmark), University of Copenhagen, Manchester University NHS Foundation Trust, MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Technical University of Denmark, University of Lausanne, NHS Greater Glasgow and Clyde, St James's University Hospital
BackgroundCongenital dyserythropoietic anaemia type I (CDA-I) is a hereditary anaemia caused by biallelic mutations in the widely expressed genes CDAN1 and C15orf41. Little is understood about either protein and it...
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