A hypomorphic mouse model of dystrophic epidermolysis bullosa reveals 
mechanisms of disease and response to fibroblast therapy

Fritsch, A.; Loeckermann, S.; Kern, J. S.; Braun, A.; Bösl, M. R.; Bley, T. A.; Schumann, H.; von Elverfeldt, D.; Paul, D.; Erlacher, M.; von Rautenfeld, D. B.; Hausser, I.; Fässler, R.; Bruckner-Tuderman, L.

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A hypomorphic mouse model of dystrophic epidermolysis bullosa reveals mechanisms of disease and response to fibroblast therapy

MPS-Authors

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Braun, A.
Fässler, Reinhard / Molecular Medicine, Max Planck Institute of Biochemistry, Max Planck Society;

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Bösl, M. R.
Fässler, Reinhard / Molecular Medicine, Max Planck Institute of Biochemistry, Max Planck Society;

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Fässler, R.
Fässler, Reinhard / Molecular Medicine, Max Planck Institute of Biochemistry, Max Planck Society;

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Fritsch, A., Loeckermann, S., Kern, J. S., Braun, A., Bösl, M. R., Bley, T. A., et al. (2008). A hypomorphic mouse model of dystrophic epidermolysis bullosa reveals mechanisms of disease and response to fibroblast therapy. Journal of Clinical Investigation, 118(5), 1669-1679.

Cite as: https://hdl.handle.net/11858/00-001M-0000-0010-5CEE-1

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