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Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients

Authors

  1. Dr C Depienne, INSERM U679, 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, Saint-Martin C, et al
Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients
Journal of Medical Genetics 2009;46:183-191.

Publication history

  • Received August 1, 2008
  • Revised September 17, 2008
  • Accepted September 26, 2008
  • First published October 17, 2008.
Online issue publication 
April 27, 2016

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2009 BMJ Publishing Group Ltd