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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Achille Iolascon

Genetica Medica

Dipartimento di Biochimica e Biotecnologie Mediche

Università Federico II




Name/email consistency: high



  • Genetica Medica, Dipartimento di Biochimica e Biotecnologie Mediche, Università Federico II, Naples, Italy. 2006 - 2009
  • Department of Scienze Biomediche, Division of Nephrology, University of Foggia, Italy. 2005


  1. Molecular basis of inherited microcytic anemia due to defects in iron acquisition or heme synthesis. Iolascon, A., De Falco, L., Beaumont, C. Haematologica (2009) [Pubmed]
  2. Microcytic anemia and hepatic iron overload in a child with compound heterozygous mutations in DMT1 (SCL11A2). Iolascon, A., d'Apolito, M., Servedio, V., Cimmino, F., Piga, A., Camaschella, C. Blood (2006) [Pubmed]
  3. Congenital nephrotic syndrome of Finnish type: detection of new nephrin mutations and prenatal diagnosis in an Italian family. Gigante, M., Greco, P., Defazio, V., Lucci, M., Margaglione, M., Gesualdo, L., Iolascon, A. Prenat. Diagn. (2005) [Pubmed]
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