Xeroderma pigmentosum (complementation group D) mutation is present in patients affected by trichothiodystrophy with photosensitivity

Author:

Stefanini M.,Lagomarsini P.,Arlett C. F.,Marinoni S.,Borrone C.,Crovato F.,Trevisan G.,Cordone G.,Nuzzo F.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Reference41 articles.

1. Andrews AD, Barret SF, Yoder FW, Robbins JH (1978) Cockayne's syndrome fibroblasts have increased sensitivity to ultraviolet light but normal rates of unscheduled DNA synthesis. J Invest Dermatol 70:237?239

2. Arlett CF, Lehmann AR, Giannelli F, Ramsay CA (1978) A human subject with a new defect in repair of ultraviolet damage. J Invest Dermatol 70:173?177

3. Baden HP, Jackson CE, Weiss L, Jimbow K, Lee L, Kubilus J, Gold RJM (1976) The physiochemical properties of hair in the BIDS syndrome. Am J Hum Genet 28:514?521

4. Braun-Falco O, Ring J, Butenandt O, Selzle D, Landthaler M (1981) Ichthyosis vulgaris, Minderwuchs, Haardysplasie, Zahnanomalien, Immundefekte, psychomotorische Retardation und Resorptions-störungen. Hautarzt 32:67?74

5. Calderon R, Gonzalez-Cantú N (1979) Kinky hair, photosensitivity, broken eyebrows and eyelashes, and non-progressive mental retardation. J Pediatr 95:1007?1008

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