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Iron status and HFE mutations in first‐degree relatives of patients with sporadic porphyria cutanea tarda, in a Mediterranean area
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Published in: | Journal of internal medicine 2005-04, Vol.257 (4), p.389-390 |
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Language: | English |
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container_end_page | 390 |
container_issue | 4 |
container_start_page | 389 |
container_title | Journal of internal medicine |
container_volume | 257 |
creator | García‐Morillo, J. S. Ramírez Lorca, R. Bernabeu‐Wittel, M. Stiefel García‐Junco, P. Pamies Andreu, E. Carneado de la Fuente, J. |
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doi_str_mv | 10.1111/j.1365-2796.2005.01462.x |
format | article |
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ispartof | Journal of internal medicine, 2005-04, Vol.257 (4), p.389-390 |
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language | eng |
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source | Wiley-Blackwell Read & Publish Collection |
subjects | Female Hemochromatosis Protein Histocompatibility Antigens Class I - genetics Humans Iron Overload - genetics Male Membrane Proteins - genetics Mutation Porphyria Cutanea Tarda - genetics |
title | Iron status and HFE mutations in first‐degree relatives of patients with sporadic porphyria cutanea tarda, in a Mediterranean area |
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