PubMed=14690602; DOI=10.1016/S1097-2765(03)00478-7
Xu-Dong Zhu, Laura J. Niedernhofer, Bernhard Kuster, Matthias Mann, Jan Hendrik Jozef Hoeijmakers, Titia de Lange;
ERCC1/XPF removes the 3' overhang from uncapped telomeres and represses formation of telomeric DNA-containing double minute chromosomes.
Mol. Cell 12:1489-1498(2003)

PubMed=17273966; DOI=10.1086/512486; PMCID=PMC1821117
Nicolaas G.J. Jaspers, Anja Raams, Margherita Cirillo Silengo, Nils Wijgers, Laura J. Niedernhofer, Andria Rasile Robinson, Giuseppina Giglia-Mari, Deborah Hoogstraten, Wim J. Kleijer, Jan Hendrik Jozef Hoeijmakers, Wim Vermeulen;
First reported patient with human ERCC1 deficiency has cerebro-oculo-facio-skeletal syndrome with a mild defect in nucleotide excision repair and severe developmental failure.
Am. J. Hum. Genet. 80:457-466(2007)

PubMed=30165384; DOI=10.1093/nar/gky774; PMCID=PMC6182131
Mariangela Sabatella, Arjan F. Theil, Cristina Ribeiro-Silva, Jana Slyskova, Karen Thijssen, Chantal Voskamp, Hannes Lans, Wim Vermeulen;
Repair protein persistence at DNA lesions characterizes XPF defect with Cockayne syndrome features.
Nucleic Acids Res. 46:9563-9577(2018)