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Recessive dystrophic epidermolysis bullosa: the origin of the c.6527insC mutation in the Spanish population

Authors

  • C. Sanchez-Jimeno,

    1. Regenerative Medicine Unit, CIEMAT, Madrid, Spain
    2. Biomedical Network Research Centre on Rare Diseases, CIBERER, Valencia, Spain
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  • N. Cuadrado-Corrales,

    1. Regenerative Medicine Unit, CIEMAT, Madrid, Spain
    2. Biomedical Network Research Centre on Rare Diseases, CIBERER, Valencia, Spain
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  • E. Aller,

    1. Biomedical Network Research Centre on Rare Diseases, CIBERER, Valencia, Spain
    2. Department of Genetics, Hospital Universitario La Fe, Valencia, Spain
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  • M. García,

    1. Biomedical Network Research Centre on Rare Diseases, CIBERER, Valencia, Spain
    2. Department of Bioengineering, Universidad Carlos III de Madrid, Madrid, Spain
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  • M.J. Escámez,

    1. Regenerative Medicine Unit, CIEMAT, Madrid, Spain
    2. Biomedical Network Research Centre on Rare Diseases, CIBERER, Valencia, Spain
    3. Department of Bioengineering, Universidad Carlos III de Madrid, Madrid, Spain
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  • N. Illera,

    1. Regenerative Medicine Unit, CIEMAT, Madrid, Spain
    2. Biomedical Network Research Centre on Rare Diseases, CIBERER, Valencia, Spain
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  • M.J. Trujillo-Tiebas,

    1. Biomedical Network Research Centre on Rare Diseases, CIBERER, Valencia, Spain
    2. Department of Genetics, Fundación Jiménez Díaz-Madrid, Madrid, Spain
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  • C. Ayuso,

    1. Biomedical Network Research Centre on Rare Diseases, CIBERER, Valencia, Spain
    2. Department of Genetics, Fundación Jiménez Díaz-Madrid, Madrid, Spain
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  • J.M. Millán,

    1. Biomedical Network Research Centre on Rare Diseases, CIBERER, Valencia, Spain
    2. Department of Genetics, Hospital Universitario La Fe, Valencia, Spain
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  • M. Del Río

    1. Biomedical Network Research Centre on Rare Diseases, CIBERER, Valencia, Spain
    2. Department of Bioengineering, Universidad Carlos III de Madrid, Madrid, Spain
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  • Funding sources: this work was supported by grants from the Spanish Ministry of Science and Innovation (MICINN) (SAF2007-61019 and SAF 2010-16976), INTRA/08/714.1 and INTA/09/758 from the Biomedical Network Research Centre on Rare Diseases (CIBERER) and S2010/BMD-2420 (CELLCAM) from Comunidad de Madrid.

  • Conflicts of interest: none declared.

  • C.S.J. and N.C.C. contributed equally to this work.

Marcela Del Rio.
E-mail: mrnechae@ing.uc3m.es

No abstract is available for this article.

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