| Literature DB >> 3982437 |
E Fischer, W Keijzer, H W Thielmann, O Popanda, E Bohnert, L Edler, E G Jung, D Bootsma.
Abstract
A new complementation group of excision-deficient xeroderma pigmentosum (XP) is described in 2 patients living in the F.R.G. Dermatological, ophthalmological and neurological symptoms of XP are presented together with DNA repair characteristics such as unscheduled DNA synthesis, colony-forming ability and alkaline elution studied in cultured fibroblasts. The results are compared to normal controls.Entities:
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Year: 1985 PMID: 3982437 DOI: 10.1016/0167-8817(85)90030-6
Source DB: PubMed Journal: Mutat Res ISSN: 0027-5107 Impact factor: 2.433