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Two individuals with features of both xeroderma pigmentosum and trichothiodystrophy highlight the complexity of the clinical outcomes of mutations in the XPD gene. |
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| Authors: | B C Broughton M Berneburg H Fawcett E M Taylor C F Arlett T Nardo M Stefanini E Menefee V H Price S Queille A Sarasin E Bohnert J Krutmann R Davidson K H Kraemer A R Lehmann |
| Affiliation: | Genome Damage and Stability Centre, University of Sussex, Falmer, Brighton BN1 9RR, UK. |
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