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LBR mutation and nuclear envelope defects in a patient affected with Reynolds syndrome
  1. Correspondence to Dr Annachiara De Sandre-Giovannoli, Laboratoire de Génétique Moléculaire, Département de Génétique Médicale, Hôpital d'Enfants la Timone, 264 Rue St. Pierre, Marseille 13385, France; annachiara.desandre{at}ap-hm.fr
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Citation

Gaudy-Marqueste C, Roll P, Esteves-Vieira V, et al
LBR mutation and nuclear envelope defects in a patient affected with Reynolds syndrome

Publication history

  • Received July 23, 2009
  • Revised November 5, 2009
  • Accepted November 9, 2009
  • First published June 3, 2010.
Online issue publication 
April 27, 2016

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