Recent Trends in WRN Gene Mutation Patterns in Individuals with Werner Syndrome
Author:
Affiliation:
1. Department of Clinical Cell Biology and Medicine; Graduate School of Medicine; Chiba University; Chiba Japan
2. Department of Medicine; Division of Diabetes; Metabolism and Endocrinology; Chiba University Hospital; Chiba Japan
Funder
Ministry of Health, Labour and Welfare
Japan Agency for Medical Research and Development
Publisher
Wiley
Subject
Geriatrics and Gerontology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/jgs.14906/fullpdf
Reference10 articles.
1. Werner syndrome: Clinical features, pathogenesis and potential therapeutic interventions;Oshima;Ageing Res Rev,2017
2. Prevalence of Werner's syndrome heterozygotes in Japan;Satoh;Lancet,1999
3. Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative Group;Yu;Am J Hum Genet,1997
4. Family analysis of Werner's syndrome: A survey of 42 Japanese families with a review of the literature;Goto;Clin Genet,1981
5. Mutation and haplotype analyses of the Werner's syndrome gene based on its genomic structure: Genetic epidemiology in the Japanese population;Matsumoto;Hum Genet,1997
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1. Renal dysfunction, malignant neoplasms, atherosclerotic cardiovascular diseases, and sarcopenia as key outcomes observed in a three-year follow-up study using the Werner Syndrome Registry;Aging;2023-05-01
2. Case Report: A novel WRN mutation in Werner syndrome patient with diabetic foot disease and myelodysplastic syndrome;Frontiers in Endocrinology;2022-07-15
3. Lifetime extension and the recent cause of death in Werner syndrome: a retrospective study from 2011 to 2020;Orphanet Journal of Rare Diseases;2022-06-13
4. Clinical and Basic Biology of Werner Syndrome, the Model Disease of Human Aging;Aging Mechanisms II;2022
5. Werner syndrome presenting as early‐onset diabetes: A case report;Journal of Diabetes Investigation;2021-10-27
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