An unusual mutation in the XPG gene leads to an internal in-frame deletion and a XP/CS complex phenotype

ISSN
1365-2133
0007-0963
Date Issued
2014
Author(s)
Lehmann, J.
Schubert, S.
Schaefer, A.
Apel, Antje
Laspe, Petra
Schiller, S.
Gratchev, Alexei
DOI
10.1111/bjd.13035