Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 8 of 8 for Cockayne "syndrome," type B
  1. ... gene provides instructions for making a protein called Cockayne syndrome A (CSA), which is involved in repairing damaged ... than 30 ERCC8 gene mutations that can cause Cockayne syndrome. This rare condition includes a variety of features, ...
  2. ... gene provides instructions for making a protein called Cockayne syndrome B (CSB). This protein is involved in repairing ... More than 60 ERCC6 gene mutations that cause Cockayne syndrome have been identified. This rare condition includes a ...
  3. ... another condition related to defective DNA repair called Cockayne syndrome. When this combination of features occurs in the same individual, it is known as xeroderma pigmentosum/Cockayne syndrome (XP/CS) complex. People with XP/CS complex ...
  4. ... another condition related to defective DNA repair called Cockayne syndrome. This combination of features is known as xeroderma pigmentosum/Cockayne syndrome (XP/CS) complex.Researchers are uncertain how variants ...
  5. ... Tamura D, DiGiovanna JJ. Xeroderma pigmentosum, trichothiodystrophy and Cockayne syndrome: a complex genotype-phenotype relationship. Neuroscience. 2007 Apr ...
  6. ... mutations in the UV-sensitive disorders: xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy. Hum Mutat. 1999;14(1):9- ...
  7. ... mutations in the UV-sensitive disorders: xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy. Hum Mutat. 1999;14(1):9- ...
  8. ... Tamura D, DiGiovanna JJ. Xeroderma pigmentosum, trichothiodystrophy and Cockayne syndrome: a complex genotype-phenotype relationship. Neuroscience. 2007 Apr ...