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

doi:10.1111/j.1365-2133.2012.10954.x

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

Fondazione IRCCS Ca' Granda- Ospedale Maggiore Policlinico

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	697-699
Number of pages	3
Journal	British Journal of Dermatology
Volume	167
Issue number	3
DOIs	https://doi.org/10.1111/j.1365-2133.2012.10954.x
Publication status	Published - Sep 2012

ASJC Scopus subject areas

Dermatology

Access to Document

10.1111/j.1365-2133.2012.10954.x

Cite this

A puzzling mutation in congenital erythropoietic porphyria and an association with β-thalassaemia trait. / Maakaron, J. E.; Abdel Malak, O.; Itani, S.; Cappellini, M. D.; Di Pierro, E.; Brancaleoni, V.; Granata, F.; Taher, A. T.

In: British Journal of Dermatology, Vol. 167, No. 3, 09.2012, p. 697-699.

Research output: Contribution to journal › Article › peer-review

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