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Original article
Mechanisms for variable expressivity of inherited SCN1A mutations causing Dravet syndrome

Authors

  1. Correspondence to Dr Christel Depienne, INSERM U975 (CRicm), Bâtiment Pharmacie 4ème étage, Groupe Hospitalier Pitié-Salpêtrière, 47 boulevard de l'hôpital,75013 Paris, France; christel.depienne{at}upmc.fr
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Citation

Depienne C, Trouillard O, Gourfinkel-An I, et al
Mechanisms for variable expressivity of inherited SCN1A mutations causing Dravet syndrome
Journal of Medical Genetics 2010;47:404-410.

Publication history

  • Received October 19, 2009
  • Revised January 27, 2010
  • Accepted February 1, 2010
  • First published June 3, 2010.
Online issue publication 
April 27, 2016

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© 2010, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.