First Japanese case of atypical progeroid syndrome/atypical Werner syndrome with heterozygousLMNAmutation-Reference-Cited by-同舟云学术

First Japanese case of atypical progeroid syndrome/atypical Werner syndrome with heterozygousLMNAmutation

Published:2014-10-20 Issue:12 Volume:41 Page:1047-1052
ISSN:0385-2407
Container-title:The Journal of Dermatology
language:en
Short-container-title:J Dermatol

Author:

Motegi Sei-ichiro¹,Yokoyama Yoko¹,Uchiyama Akihiko¹,Ogino Sachiko¹,Takeuchi Yuko¹,Yamada Kazuya¹,Hattori Tomoyasu¹,Hashizume Hiroaki²,Ishikawa Yuichi³,Goto Makoto⁴⁵,Ishikawa Osamu¹

Affiliation:

1. Department of Dermatology; Gunma University Graduate School of Medicine; Maebashi Japan

2. Department of Medicine and Molecular Science; Gunma University Graduate School of Medicine; Maebashi Japan

3. Department of Pathology; Institute of Cancer Research; Japanese Foundation for Cancer Research; Tokyo Japan

4. Division of Orthopedic Surgery and Rheumatology; East Medical Center; Tokyo Women's Medical University; Tokyo Japan

5. Division of Anti-aging and Longevity Sciences; Department of Clinical Engineering; Faculty of Medical Engineering; Toin University of Yokohama; Yokohama Kanagawa Japan

Publisher

Wiley

Subject

Dermatology,General Medicine

Reference17 articles.

1. Genetic linkage of Werner's syndrome to five markers on chromosome 8;Goto;Nature,1992

2. LMNA mutations in atypical Werner's syndrome;Chen;Lancet,2003

3. Search and Insights into novel genetic alterations leading to classical and atypical Werner syndrome;Oshima;Gerontology,2014

4. Triple primary sarcoma in Werner syndrome with a novel mutation;Nakamura;Rheumatology (Oxford),2003

5. Identification of mutational hot spots in LMNA encoding lamin A/C in patients with familial dilated cardiomyopathy;Perrot;Basic Res Cardiol,2009

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