Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3.

Documenti analoghi

• Correction of xeroderma pigmentosum repair defect by basal transcription factor BTF2 (TFIIH).
  di: van Vuuren, A J, et al.
  Pubblicazione: (1994)
• Evidence for a repair enzyme complex involving ERCC1 and complementing activities of ERCC4, ERCC11 and xeroderma pigmentosum group F.
  di: van Vuuren, A J, et al.
  Pubblicazione: (1993)
• Correction of the DNA repair defect in xeroderma pigmentosum group E by injection of a DNA damage-binding protein.
  di: Keeney, S, et al.
  Pubblicazione: (1994)
• Structure and expression of the human XPBC/ERCC-3 gene involved in DNA repair disorders xeroderma pigmentosum and Cockayne's syndrome.
  di: Weeda, G, et al.
  Pubblicazione: (1991)
• Xeroderma pigmentosum complementation group G associated with Cockayne syndrome.
  di: Vermeulen, W, et al.
  Pubblicazione: (1993)