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(1997) Analysis of helicase gene mutations in Japanese Werner\u2019s syndrome patients. Hum Genet 99: 191\u2013193.","DOI":"10.1007\/s004390050336"},{"key":"2","doi-asserted-by":"crossref","unstructured":"2 Coppede F (2012) Premature aging syndrome. Adv Exp Med Biol 724: 317\u2013331.","DOI":"10.1007\/978-1-4614-0653-2_24"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3 Oshima J, Hisama FM (2014) Search and insights into novel genetic alterations leading to classical and atypical Werner syndrome. Gerontology 60: 239\u2013246.","DOI":"10.1159\/000356030"},{"key":"4","doi-asserted-by":"publisher","unstructured":"4 Chen L, Lee L, Kudlow BA, Dos Santos HG, Sletvold O, et al. (2003) LMNA mutations in atypical Werner\u2019s syndrome. Lancet 362: 440\u2013445.","DOI":"10.1016\/S0140-6736(03)14069-X"},{"key":"5","doi-asserted-by":"crossref","unstructured":"5 Jacob KN, Baptista F, dos Santos HG, Oshima J, Agarwal AK, et al. (2005) Phenotypic heterogeneity in body fat distribution in patients with atypical Werner\u2019s syndrome due to heterozygous Arg133Leu lamin A\/C mutation. J Clin Endocrinol Metab 90: 6699\u20136706.","DOI":"10.1210\/jc.2005-0939"},{"key":"6","unstructured":"6 Oshima J, Martin GM, Hisama FM (2002) Werner syndrome. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, <i>et al.<\/i> (eds). GeneReviews<sup>\u00ae<\/sup>. Seattle (WA), University of Washington, Seattle: 1993\u20132019."},{"key":"7","doi-asserted-by":"crossref","unstructured":"7 Takemoto M, Mori S, Kuzuya M, Yoshimoto S, Shimamoto A, et al. (2013) Diagnostic criteria for Werner syndrome based on Japanese nationwide epidemiological survey. Geriatr Gerontol Int 13: 475\u2013481.","DOI":"10.1111\/j.1447-0594.2012.00913.x"},{"key":"8","doi-asserted-by":"crossref","unstructured":"8 Ishiyama A, Iida A, Hayashi S, Komaki H, Sasaki M, et al. 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