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APA Citation
Schäfer, A., Gratchev, A., Seebode, C., Hofmann, L., Schubert, S., Laspe, P., Apel, A., Ohlenbusch, A., Tzvetkov, M., Weishaupt, C., Oji, V., Schön, M. P., & Emmert, S. (n.d.). functional and molecular genetic analyses of nine newly identified XPD‐deficient patients reveal a novel mutation resulting in TTD as well as in XP/CS complex phenotypes. Experimental dermatology, 22(7), 486–489. http://access.bl.uk/ark:/81055/vdc_100024542196.0x000024