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author Depienne, Christel
Bouteiller, Delphine
Keren, Boris
Cheuret, Emmanuel
Poirier, Karine
Trouillard, Oriane
Benyahia, Baya
Quelin, Chloé
Carpentier, Wassila
Julia, Sophie
Afenjar, Alexandra
Gautier, Agnès
Rivier, François
Meyer, Sophie
Berquin, Patrick
Hélias, Marie
Py, Isabelle
Rivera, Serge
Bahi-Buisson, Nadia
Gourfinkel-An, Isabelle
Cazeneuve, Cécile
Ruberg, Merle
Brice, Alexis
Nabbout, Rima
LeGuern, Eric
author_facet Depienne, Christel
Bouteiller, Delphine
Keren, Boris
Cheuret, Emmanuel
Poirier, Karine
Trouillard, Oriane
Benyahia, Baya
Quelin, Chloé
Carpentier, Wassila
Julia, Sophie
Afenjar, Alexandra
Gautier, Agnès
Rivier, François
Meyer, Sophie
Berquin, Patrick
Hélias, Marie
Py, Isabelle
Rivera, Serge
Bahi-Buisson, Nadia
Gourfinkel-An, Isabelle
Cazeneuve, Cécile
Ruberg, Merle
Brice, Alexis
Nabbout, Rima
LeGuern, Eric
author_sort Depienne, Christel
collection PubMed
description
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institution National Center for Biotechnology Information
language English
publishDate 2009
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-27067102009-07-09 Correction: Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females Depienne, Christel Bouteiller, Delphine Keren, Boris Cheuret, Emmanuel Poirier, Karine Trouillard, Oriane Benyahia, Baya Quelin, Chloé Carpentier, Wassila Julia, Sophie Afenjar, Alexandra Gautier, Agnès Rivier, François Meyer, Sophie Berquin, Patrick Hélias, Marie Py, Isabelle Rivera, Serge Bahi-Buisson, Nadia Gourfinkel-An, Isabelle Cazeneuve, Cécile Ruberg, Merle Brice, Alexis Nabbout, Rima LeGuern, Eric PLoS Genet Correction Public Library of Science 2009-04-03 /pmc/articles/PMC2706710/ http://dx.doi.org/10.1371/annotation/314060d5-06da-46e0-b9e4-57194e8ece3a Text en Public Library of Science. http://creativecommons.org/licenses/by/4.0/ 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 properly credited.
spellingShingle Correction
Depienne, Christel
Bouteiller, Delphine
Keren, Boris
Cheuret, Emmanuel
Poirier, Karine
Trouillard, Oriane
Benyahia, Baya
Quelin, Chloé
Carpentier, Wassila
Julia, Sophie
Afenjar, Alexandra
Gautier, Agnès
Rivier, François
Meyer, Sophie
Berquin, Patrick
Hélias, Marie
Py, Isabelle
Rivera, Serge
Bahi-Buisson, Nadia
Gourfinkel-An, Isabelle
Cazeneuve, Cécile
Ruberg, Merle
Brice, Alexis
Nabbout, Rima
LeGuern, Eric
Correction: Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females
title Correction: Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females
title_full Correction: Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females
title_fullStr Correction: Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females
title_full_unstemmed Correction: Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females
title_short Correction: Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females
title_sort correction: sporadic infantile epileptic encephalopathy caused by mutations in pcdh19 resembles dravet syndrome but mainly affects females
topic Correction
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2706710/
http://dx.doi.org/10.1371/annotation/314060d5-06da-46e0-b9e4-57194e8ece3a
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