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.
Citation: Depienne C, Bouteiller D, Keren B, Cheuret E, Poirier K, Trouillard O, et al. (2009) Correction: Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females. PLoS Genet 5(4): 10.1371/annotation/314060d5-06da-46e0-b9e4-57194e8ece3a. https://doi.org/10.1371/annotation/314060d5-06da-46e0-b9e4-57194e8ece3a
Published: April 03, 2009
Copyright: © 2009 . This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Competing interests: No competing interests declared.