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APA Citation
Lehmann, J., Schubert, S., Schäfer, A., Apel, A., Laspe, P., Schiller, S., Ohlenbusch, A., Gratchev, A., & Emmert, S. (n.d.). an unusual mutation in the XPG gene leads to an internal in‐frame deletion and a XP/CS complex phenotype. British journal of dermatology, 171, 903–905. http://access.bl.uk/ark:/81055/vdc_100172527225.0x000054