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Correction

Correction: Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females

  • Christel Depienne,
  • Delphine Bouteiller,
  • Boris Keren,
  • Emmanuel Cheuret,
  • Karine Poirier,
  • Oriane Trouillard,
  • Baya Benyahia,
  • Chloé Quelin,
  • Wassila Carpentier,
  • Sophie Julia,
  • Alexandra Afenjar,
  • Agnès Gautier,
  • François Rivier,
  • Sophie Meyer,
  • Patrick Berquin,
  • Marie Hélias,
  • Isabelle Py,
  • Serge Rivera,
  • Nadia Bahi-Buisson,
  • Isabelle Gourfinkel-An,
  • Cécile Cazeneuve,
  • Merle Ruberg,
  • Alexis Brice,
  • Rima Nabbout,
  • Eric LeGuern
  • Published: April 03, 2009
  • DOI: 10.1371/annotation/314060d5-06da-46e0-b9e4-57194e8ece3a

The affiliations for the 20th author, Isabelle Gourfinkel-An, and the 24th author, Rima Nabbout, were incorrect. Dr. Gourfinkel-An is affiliated with: INSERM U975 (Ex-U679), Paris, France; Plate-forme Post-Génomique P3S, UPMC, Faculté de Médecine, Paris, France; and Centre de Référence Épilepsies Rares, Paris, France. Dr. Nabbout is affiliated with: Département de Neuropédiatrie, AP-HP, Hôpital Necker-Enfants Malades, Paris-Descartes, Paris, France; and Centre de Référence Épilepsies Rares, Paris, France.