Functional and molecular genetic analyses of 9 newly identified XPD-deficient patients reveal a novel mutation resulting in TTD as well as in XP/CS complex phenotypes
2013 | conference abstract. A publication with affiliation to the University of Göttingen.
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Functional and molecular genetic analyses of 9 newly identified XPD-deficient patients reveal a novel mutation resulting in TTD as well as in XP/CS complex phenotypes
Emmert, S.; Schaefer, A.; Gratchev, A.; Seebode, C.; Hofmann, L.; Schubert, S. & Laspe, P. et al. (2013)
JDDG Journal der Deutschen Dermatologischen Gesellschaft, 11(9)
Hoboken: Wiley-blackwell.
Documents & Media
Details
- Authors
- Emmert, Steffen; Schaefer, A.; Gratchev, Alexei; Seebode, Christina; Hofmann, L.; Schubert, S.; Laspe, Petra; Apel, Antje; Ohlenbusch, Andreas; Tzvetkov, Mladen Vassilev; Weishaupt, Carsten; Oji, Vinzenz; Schoen, Michael Peter
- Issue Date
- 2013
- Status
- published
- Publisher
- Wiley-blackwell
- Journal
- JDDG Journal der Deutschen Dermatologischen Gesellschaft
- ISSN
- 1610-0379
- Extent
- 942
