Novel LMNA Mutation in Atypical Werner Syndrome Presenting With Ischemic Disease-Reference-Cited by-同舟云学术

Novel LMNA Mutation in Atypical Werner Syndrome Presenting With Ischemic Disease

Published:2009-02 Issue:2 Volume:40 Page:
ISSN:0039-2499
Container-title:Stroke
language:en
Short-container-title:Stroke

Author:

Renard Dimitri¹,Fourcade Genevieve¹,Milhaud Didier¹,Bessis Didier¹,Esteves-Vieira Vera¹,Boyer Amandine¹,Roll Patrice¹,Bourgeois Patrice¹,Levy Nicolas¹,De Sandre-Giovannoli Annachiara¹

Affiliation:

1. From Department of Neurology (D.R., G.F., D.M.), Department of Dermatology (D.B.), CHU Montpellier, Hôpital Gui de Chauliac, Montpellier, France; Laboratoire de Génétique Moléculaire (V.E.-V., A.B., P.B., N.L., A.D.S.-G.), Département de Génétique Médicale, Hôpital d’Enfants la Timone, Marseille, France; Laboratoire de Biologie Cellulaire (P.R.), Hôpital la Conception, Marseille, France; INSERM UMR_S910 (N.L., A.D.S.-G.), Faculté de Médecine de Marseille, Marseille.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Advanced and Specialised Nursing,Cardiology and Cardiovascular Medicine,Clinical Neurology

Reference7 articles.

1. Werner's Syndrome

2. Positional Cloning of the Werner's Syndrome Gene

3. LMNA mutations in atypical Werner's syndrome

4. Genomic instability in laminopathy-based premature aging

5. Accelerated ageing in mice deficient in Zmpste24 protease is linked to p53 signalling activation

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