DNA repair, ERCC3, Neurodegeneration, Skin cancer, TFIIH, Transcription, XPB
dx.doi.org/10.1002/humu.20392, hdl.handle.net/1765/67949
Human Mutation
Department of Molecular Genetics

Oh, K.-S, Khan, S.G, Jaspers, N.G.J, Raams, A, Ueda, T, Lehmann, A.R, … Kraemer, K.H. (2006). Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): Xeroderma pigmentosum without and with Cockayne syndrome. Human Mutation, 27(11), 1092–1103. doi:10.1002/humu.20392