Hat mitgewirkt an:
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Generation and genetic repair of two human induced pluripotent stem cell lines from patients with Epidermolysis Bullosa simplex associated with a heterozygous mutation in the translation initiation...
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Emergency management in epidermolysis bullosa: consensus clinical recommendations from the European reference network for rare skin diseases
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Effect of small molecule eRF3 degraders on premature termination codon readthrough
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Kindler syndrome in a patient with colitis and primary sclerosing cholangitis : : coincidence or association?