Open AccessCorrection: Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females
Author(s) -
Christel Depienne,
Delphine Bouteiller,
Boris Keren,
Emmanuel Cheuret,
Karine Poirier,
Oriane Trouillard,
B. Benyahia,
Chloé Quēlin,
Wassila Carpentier,
Sophie Julia,
Alexandra Afenjar,
Agnès Gautier,
François Rivier,
Sophie Meyer,
Patrick Berquin,
Marie Hélias,
Isabelle Py,
Eleanor Rivera,
Nadia BahiBuisson,
Isabelle GourfinkelAn,
Cécile Cazeneuve,
Merle Ruberg,
Alexis Brice,
Rima Nabbout,
Éric Leguern
Publication year - 2009
Publication title -
plos genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.587
H-Index - 233
eISSN - 1553-7404
pISSN - 1553-7390
DOI - 10.1371/annotation/314060d5-06da-46e0-b9e4-57194e8ece3a
Subject(s) - dravet syndrome , biology , epilepsy , encephalopathy , genetics , pediatrics , bioinformatics , medicine , neuroscience