1. Yu CE, Oshima J, Goddard KA, Miki T, Nakura J, Ogihara T, Poot M, Hoehn H, Fraccaro M, Piussan C, Fu YM, Mulligan J, Ouis S, Martin GM: Linkage disequilibrium and haplotype studies of chromosome 8p11.1-21.1 markers and Werner syndrome. Am J Hum Genet. 1994, 55: 356-364.
2. Fukuchi K, Martin GM, Monnat RJ: Mutator phenotype Werner syndrome is characterized by extensive deletion. Proc Natl Acad Sci USA. 1989, 86: 5893-5897. 10.1073/pnas.86.15.5893.
3. Harrigan JA, Wilson DM, Prasad R, Opresko PL, Beck G, May A, Wilson SH, Bohr VA: The Werner syndrome protein operates in base excision repair and cooperates with DNA polymerase beta. Nucleic Acids Res. 2006, 34: 745-754. 10.1093/nar/gkj475.
4. Martin GM: Genetic syndromes in man with potential relevance to the pathology of aging. Birth Defects Orig Artic Ser. 1978, 14: 5-39.
5. Goto M, Miller RW, Ishikawa Y, Sugano H: Excess of rare cancers in Werner syndrome (Adult progeria). Cancer Epidem Biomarkers Prev. 1996, 5: 239-246.