Entry details

Murai et al. (2001) "Early postnatal ataxia and abnormal cerebellar development in mice lacking Xeroderma pigmentosum Group A and Cockayne syndrome Group B DNA repair genes." Proc. Natl. Acad. Sci. U.S.A. 98(23):13379-13384 (PubMed)

Cited by (in linked databases)

  1. ERCC6, excision repair cross-complementing rodent repair deficiency, complementation group 6 GenAge: Human Ageing-Associated Genes
  2. XPA, xeroderma pigmentosum, complementation group A GenAge: Human Ageing-Associated Genes