An unusual mutation in the XPG gene leads to an internal in-frame deletion and a XP/CS complex phenotype
2014 | conference abstract. A publication with affiliation to the University of Göttingen.
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An unusual mutation in the XPG gene leads to an internal in-frame deletion and a XP/CS complex phenotype
Lehmann, J.; Schubert, S.; Schaefer, A.; Apel, A.; Laspe, P.; Schiller, S. & Ohlenbusch, A. et al. (2014)
Experimental Dermatology, 23(3) 41st Annual Meeting of the Arbeitsgemeinschaft-Dermatologische-Forschung (ADF), Cologne, GERMANY.
Hoboken: Wiley-blackwell.
Documents & Media
Details
- Authors
- Lehmann, J.; Schubert, S.; Schaefer, A.; Apel, Antje; Laspe, Petra; Schiller, S.; Ohlenbusch, Andreas; Gratchev, Alexei; Emmert, Steffen
- Issue Date
- 2014
- Status
- published
- Publisher
- Wiley-blackwell
- Journal
- Experimental Dermatology
- Conference
- 41st Annual Meeting of the Arbeitsgemeinschaft-Dermatologische-Forschung (ADF)
- Conference Place
- Cologne, GERMANY
- ISSN
- 1600-0625; 0906-6705
- Extent
- E22
