Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): Xeroderma pigmentosum without and with Cockayne syndrome

Additional Metadata
Keywords	DNA repair, ERCC3, Neurodegeneration, Skin cancer, TFIIH, Transcription, XPB
Persistent URL	doi.org/10.1002/humu.20392, hdl.handle.net/1765/67949
Journal	Human Mutation
Organisation	Department of Molecular Genetics
Citation APA Style AAA Style APA Style Cell Style Chicago Style Harvard Style IEEE Style MLA Style Nature Style Vancouver Style American-Institute-of-Physics Style Council-of-Science-Editors Style BibTex Format Endnote Format RIS Format CSL Format DOIs only Format	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

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