Werner Syndrome: Characterization of Mutations in the WRN Gene in an Affected Family-Reference-Cited by-同舟云学术

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Werner Syndrome: Characterization of Mutations in the WRN Gene in an Affected Family

Published:1997 Issue:6 Volume:5 Page:364-370
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Meisslitzer Claudia,Ruppitsch Werner,Weirich-Schwaiger Helga,Weirich Harald G.,Jabkowsky Jörg,Klein Georg,Schweiger Manfred,Hirsch-Kauffmann Monica

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Cited by 15 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Homologous recombination and maintenance of genome integrity: Cancer and aging through the prism of human RecQ helicases;Mechanisms of Ageing and Development;2008-07

2. Poikiloderma, tendon contracture and pulmonary fibrosis: a new autosomal dominant syndrome?;British Journal of Dermatology;2006-08-10

3. The spectrum ofWRNmutations in Werner syndrome patients;Human Mutation;2006-06

4. The Werner Syndrome: A Model for the Study of Human Aging;Annals of the New York Academy of Sciences;2006-01-25

5. Nuclear deformation characterizes Werner syndrome cells;Cell Biology International;2005-12

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