A ninth complementation group in xeroderma pigmentosum, XP I
- PMID: 3982437
- DOI: 10.1016/0167-8817(85)90030-6
A ninth complementation group in xeroderma pigmentosum, XP I
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.
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