Diabetes mellitus coexisted with progeria: a case report of atypical Werner syndrome with novel LMNA mutations and literature review
Author:
Affiliation:
1. The First Hospital of Jilin University, Changchun Jilin, 130021, China
Publisher
Japan Endocrine Society
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Link
https://www.jstage.jst.go.jp/article/endocrj/66/11/66_EJ19-0014/_pdf
Reference29 articles.
1. 1 Goto M, Imamura O, Kuromitsu J, Matsumoto T, Yamabe Y, et al. (1997) Analysis of helicase gene mutations in Japanese Werner’s syndrome patients. Hum Genet 99: 191–193.
2. 2 Coppede F (2012) Premature aging syndrome. Adv Exp Med Biol 724: 317–331.
3. 3 Oshima J, Hisama FM (2014) Search and insights into novel genetic alterations leading to classical and atypical Werner syndrome. Gerontology 60: 239–246.
4. 4 Chen L, Lee L, Kudlow BA, Dos Santos HG, Sletvold O, et al. (2003) LMNA mutations in atypical Werner’s syndrome. Lancet 362: 440–445.
5. 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’s syndrome due to heterozygous Arg133Leu lamin A/C mutation. J Clin Endocrinol Metab 90: 6699–6706.
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