Entry details

Sijbers et al. (1998) "Homozygous R788W point mutation in the XPF gene of a patient with xeroderma pigmentosum and late-onset neurologic disease." J. Invest. Dermatol. 110(5):832-836 (PubMed)

Cited by (in linked databases)

  1. ERCC4, excision repair cross-complementing rodent repair deficiency, complementation group 4 GenAge: Human Ageing-Associated Genes