human homolog binds WRN, a member of the RecQ family of DNA helicases that is mutated in Werner syndrome; may contribute to the premature aging phenotype in Werner syndrome [RGD, Feb 2006]
human homolog binds WRN, a member of the RecQ family of DNA helicases that is mutated in Werner syndrome; may contribute to the premature aging phenotype in Werner syndrome [RGD, Feb 2006]