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Correction: IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients.
Mignot, Cyril; McMahon, Aoife C; Bar, Claire; Campeau, Philippe M; Davidson, Claire; Buratti, Julien; Nava, Caroline; Jacquemont, Marie-Line; Tallot, Marilyn; Milh, Mathieu; Edery, Patrick; Marzin, Pauline; Barcia, Giulia; Barnerias, Christine; Besmond, Claude; Bienvenu, Thierry; Bruel, Ange-Line; Brunga, Ledia; Ceulemans, Berten; Coubes, Christine; Cristancho, Ana G; Cunningham, Fiona; Dehouck, Marie-Bertille; Donner, Elizabeth J; Duban-Bedu, Bénédicte; Dubourg, Christèle; Gardella, Elena; Gauthier, Julie; Geneviève, David; Gobin-Limballe, Stéphanie; Goldberg, Ethan M; Hagebeuk, Eveline; Hamdan, Fadi F; Hancárová, Miroslava; Hubert, Laurence; Ioos, Christine; Ichikawa, Shoji; Janssens, Sandra; Journel, Hubert; Kaminska, Anna; Keren, Boris; Koopmans, Marije; Lacoste, Caroline; Lassuthová, Petra; Lederer, Damien; Lehalle, Daphné; Marjanovic, Dragan; Métreau, Julia; Michaud, Jacques L; Miller, Kathryn.
Afiliação
  • Mignot C; INSERM, U 1127, CNRS UMR 7225, Sorbonne Universites, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle epiniere, ICM, Paris, France. cyril.mignot@aphp.fr.
  • McMahon AC; APHP, Hôpital Pitie-Salpetriere, Departement de Genetique et de Cytogenetique; Centre de Reference Deficience Intellectuelle de Causes Rares, GRC UPMC «Deficience Intellectuelle et Autisme¼, Paris, France. cyril.mignot@aphp.fr.
  • Bar C; European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.
  • Campeau PM; APHP, Reference Centre for Rare Epilepsies, Necker-Enfants Malades Hospital, Imagine Institute, Paris Descartes University, Paris, France.
  • Davidson C; INSERM U1163, Imagine Institute, Paris, France.
  • Buratti J; Paris Descartes University, Paris, France.
  • Nava C; Division of Medical Genetics, Department of Pediatrics, CHU Sainte-Justine and University of Montreal, Montreal, QC, Canada.
  • Jacquemont ML; European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.
  • Tallot M; APHP, Hôpital Pitie-Salpetriere, Departement de Genetique et de Cytogenetique; Centre de Reference Deficience Intellectuelle de Causes Rares, GRC UPMC «Deficience Intellectuelle et Autisme¼, Paris, France.
  • Milh M; INSERM, U 1127, CNRS UMR 7225, Sorbonne Universites, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle epiniere, ICM, Paris, France.
  • Edery P; APHP, Hôpital Pitie-Salpetriere, Departement de Genetique et de Cytogenetique; Centre de Reference Deficience Intellectuelle de Causes Rares, GRC UPMC «Deficience Intellectuelle et Autisme¼, Paris, France.
  • Marzin P; CHU La Reunion-Groupe Hospitalier Sud Reunion, La Reunion, France.
  • Barcia G; CHU La Reunion-Groupe Hospitalier Sud Reunion, La Reunion, France.
  • Barnerias C; APHM, Hôpital d'Enfants de La Timone, Service de Neurologie Pediatrique, centre de reference deficiences intellectuelles de cause rare, Marseille, France.
  • Besmond C; Aix Marseille University, INSERM, MMG, UMR-S 1251, Faculte de medecine, Marseille, France.
  • Bienvenu T; Service de Genetique, Centre de Reference Anomalies du Developpement, Hospices Civils de Lyon, Bron, France.
  • Bruel AL; INSERM U1028, CNRS UMR5292, Centre de Recherche en Neurosciences de Lyon, GENDEV Team, Universite Claude Bernard Lyon 1, Bron, France.
  • Brunga L; Claude Bernard Lyon I University, Lyon, France.
  • Ceulemans B; APHP, Hôpital Pitie-Salpetriere, Departement de Genetique et de Cytogenetique; Centre de Reference Deficience Intellectuelle de Causes Rares, GRC UPMC «Deficience Intellectuelle et Autisme¼, Paris, France.
  • Coubes C; INSERM U1163, Imagine Institute, Paris, France.
  • Cristancho AG; Paris Descartes University, Paris, France.
  • Cunningham F; APHP, Service de genetique medicale, Necker- Enfants Malades Hospital, Imagine Institute, Paris Descartes University, Paris, France.
  • Dehouck MB; APHP, Unite fonctionnelle de Neurologie, Necker-Enfants Malades Hospital, Imagine Institute, Paris Descartes University, Paris, France.
  • Donner EJ; INSERM U1163, Imagine Institute, Paris, France.
  • Duban-Bedu B; Paris Descartes University, Paris, France.
  • Dubourg C; APHP, Laboratoire de Genetique et Biologie Moleculaires, Hôpital Cochin, HUPC, Paris, France.
  • Gardella E; Universite Paris Descartes Paris, Institut de Psychiatrie et de Neurosciences de Paris, Inserm U894, Paris, France.
  • Gauthier J; FHU-TRANSLAD, Universite de Bourgogne/CHU Dijon, Dijon, France.
  • Geneviève D; INSERM UMR 1231 GAD team, Genetics of Developmental disorders, Universite de Bourgogne-Franche Comte, Dijon, France.
  • Gobin-Limballe S; Division of Neurology, Department of Paediatrics, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
  • Goldberg EM; Department of Pediatric Neurology, University Hospital and University of Antwerp, Antwerp, Belgium.
  • Hagebeuk E; Departement de Genetique Medicale, Maladies rares et Medecine Personnalisee, CHU de Montpellier, Montpellier, France.
  • Hamdan FF; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Hancárová M; European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.
  • Hubert L; Centre de Genetique Chromosomique, Hôpital St-Vincent-de-Paul, GHICL, Lille, France.
  • Ioos C; Division of Neurology, Department of Paediatrics, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
  • Ichikawa S; Centre de Genetique Chromosomique, Hôpital St-Vincent-de-Paul, GHICL, Lille, France.
  • Janssens S; CHU Rennes, Service de Genetique Moleculaire et Genomique, Rennes, France.
  • Journel H; Danish Epilepsy Centre Filadelfia, Dianalund, Denmark.
  • Kaminska A; Institute for Regional Health Services, University of Southern Denmark, Odense, Denmark.
  • Keren B; Division of Medical Genetics, Department of Pediatrics, CHU Sainte-Justine and University of Montreal, Montreal, QC, Canada.
  • Koopmans M; Departement de Genetique Medicale, Maladies rares et Medecine Personnalisee, CHU de Montpellier, Montpellier, France.
  • Lacoste C; INSERM, U1183, Montpellier, France.
  • Lassuthová P; APHP, Service de genetique medicale, Necker- Enfants Malades Hospital, Imagine Institute, Paris Descartes University, Paris, France.
  • Lederer D; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Lehalle D; Stichting Epilepsie Instellingen Nederland, SEIN, Zwolle, The Netherlands.
  • Marjanovic D; Division of Medical Genetics, Department of Pediatrics, CHU Sainte-Justine and University of Montreal, Montreal, QC, Canada.
  • Métreau J; Department of Biology and Medical Genetics, Charles University 2nd Faculty of Medicine and University Hospital Motol, Prague, Czech Republic.
  • Michaud JL; INSERM U1163, Imagine Institute, Paris, France.
  • Miller K; Paris Descartes University, Paris, France.
Genet Med ; 21(8): 1897-1898, 2019 Aug.
Article em En | MEDLINE | ID: mdl-30279470
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article