Volume 160, Issue 6 pp. 1330-1334

A homozygous mutation in the ferrochelatase gene underlies erythropoietic protoporphyria associated with palmar keratoderma

M. Méndez

M. Méndez

Research Center, Hospital Universitario 12 de Octubre, Madrid, Spain

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P. Poblete-Gutiérrez

P. Poblete-Gutiérrez

Department of Dermatology, Maastricht University Center for Molecular Dermatology, Euregional Porphyria Center Maastricht and GROW – School for Oncology and Developmental Biology, University Medical Center Maastricht, P. Debyelaan 25, PO Box 5800, 6202 AZ Maastricht, the Netherlands

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M.-J. Morán-Jiménez

M.-J. Morán-Jiménez

Research Center, Hospital Universitario 12 de Octubre, Madrid, Spain

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M.-E. Rodriguez

M.-E. Rodriguez

Research Center, Hospital Universitario 12 de Octubre, Madrid, Spain

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M.-C. Garrido-Astray

M.-C. Garrido-Astray

Research Center, Hospital Universitario 12 de Octubre, Madrid, Spain

Department of Morphological Sciences and Physiology, European University of Madrid, Madrid, Spain

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A. Fontanellas

A. Fontanellas

Gene Therapy and Hepatology Area, Centre for Applied Medical Research, University of Navarra, Spain

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J. Frank

J. Frank

Department of Dermatology, Maastricht University Center for Molecular Dermatology, Euregional Porphyria Center Maastricht and GROW – School for Oncology and Developmental Biology, University Medical Center Maastricht, P. Debyelaan 25, PO Box 5800, 6202 AZ Maastricht, the Netherlands

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R.E. De Salamanca

R.E. De Salamanca

Research Center, Hospital Universitario 12 de Octubre, Madrid, Spain

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First published: 12 May 2009
Citations: 11
Jorge Frank.
E-mail:
[email protected]

Conflicts of interest:none declared.

M.M. and P.P.-G. contributed equally to this manuscript. J.F. and R.E.deS. share senior authorship.

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