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

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

Original language	English (US)
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
State	Published - Sep 2012
Externally published	Yes

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title = "A puzzling mutation in congenital erythropoietic porphyria and an association with β-thalassaemia trait",

author = "Maakaron, {J. E.} and {Abdel Malak}, O. and S. Itani and Cappellini, {M. D.} and {Di Pierro}, E. and V. Brancaleoni and F. Granata and Taher, {A. T.}",

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AU - Maakaron, J. E.

AU - Abdel Malak, O.

AU - Itani, S.

AU - Cappellini, M. D.

AU - Di Pierro, E.

AU - Brancaleoni, V.

AU - Granata, F.

AU - Taher, A. T.

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DO - 10.1111/j.1365-2133.2012.10954.x

M3 - Letter

C2 - 22429022

AN - SCOPUS:84865596348

SN - 0007-0963

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EP - 699

JO - British Journal of Dermatology

JF - British Journal of Dermatology

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ER -

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

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