Research ArticleMuscular Dystrophy

Laminopathies disrupt epigenomic developmental programs and cell fate

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Science Translational Medicine  20 Apr 2016:
Vol. 8, Issue 335, pp. 335ra58
DOI: 10.1126/scitranslmed.aad4991

Article Information

vol. 8 no. 335 335ra58

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History: 
  • Received for publication September 21, 2015
  • Accepted for publication February 28, 2016
  • .

Author Information

  1. Jelena Perovanovic1,2,
  2. Stefania Dell’Orso3,
  3. Viola F. Gnochi1,
  4. Jyoti K. Jaiswal1,2,
  5. Vittorio Sartorelli3,
  6. Corinne Vigouroux4,5,6,7,
  7. Kamel Mamchaoui8,
  8. Vincent Mouly8,
  9. Gisèle Bonne8 and
  10. Eric P. Hoffman1,2,*,
  1. 1Center for Genetic Medicine Research, Children’s National Medical Center, Washington, DC 20010, USA.
  2. 2Department of Integrative Systems Biology, The George Washington University School of Medicine and Health Sciences, Washington, DC 20010, USA.
  3. 3Laboratory of Muscle Stem Cells and Gene Regulation, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD 20852, USA.
  4. 4Assistance Publique–Hôpitaux de Paris (AP-HP), Hôpital Saint-Antoine, Laboratoire Commun de Biologie et Génétique Moléculaires, F-75012 Paris, France.
  5. 5INSERM UMR_S938, Centre de Recherche Saint-Antoine, F-75012 Paris, France.
  6. 6Sorbonne Universités, UPMC (Université Pierre et Marie Curie) Univ Paris 06, UMR_S938, F-75005 Paris, France.
  7. 7ICAN (Institute of Cardiometabolism and Nutrition), F-75013 Paris, France.
  8. 8Sorbonne Universités, UPMC Univ Paris 06, INSERM UMRS974, CNRS FRE3617, Center for Research in Myology, F-75013 Paris, France.
  1. Corresponding author. E-mail: ehoffman{at}binghamton.edu
    • * Present address: SUNY Binghamton School of Pharmacy, 4400 Vestal Parkway East Binghamton, NY 13902, USA.

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