A puzzling mutation in congenital erythropoietic porphyria and an association with β-thalassaemia trait

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 journalArticlepeer-review

Original languageEnglish
Pages (from-to)697-699
Number of pages3
JournalBritish Journal of Dermatology
Volume167
Issue number3
DOIs
Publication statusPublished - Sep 2012

ASJC Scopus subject areas

  • Dermatology

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