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Dive into the research topics of 'A puzzling mutation in congenital erythropoietic porphyria and an association with β-thalassaemia trait'. Together they form a unique fingerprint.- Sort by
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J. E. Maakaron, O. Abdel Malak, S. Itani, M. D. Cappellini, E. Di Pierro, V. Brancaleoni, F. Granata, A. T. Taher
Research output: Contribution to journal › Letter › peer-review