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Reply: The expanding neurological phenotype of DNM1L-related disorders.
Gerber, Sylvie; Charif, Majida; Chevrollier, Arnaud; Chaumette, Tanguy; Angebault, Claire; Kane, Selma; Paris, Aurélien; Alban, Jennifer; Quiles, Mélanie; Delettre, Cécile; Bonneau, Dominique; Procaccio, Vincent; Amati-Bonneau, Patrizia; Reynier, Pascal; Leruez, Stéphanie; Calmon, Raphael; Boddaert, Nathalie; Funalot, Benoit; Rio, Marlène; Bouccara, Didier; Meunier, Isabelle; Sesaki, Hiromi; Kaplan, Josseline; Hamel, Christian P; Rozet, Jean-Michel; Lenaers, Guy.
Affiliation
  • Gerber S; Laboratory of Genetics in Ophthalmology, INSERM UMR1163, Imagine - Institute of Genetic Diseases, Paris Descartes University, 75015 Paris, France.
  • Charif M; MitoLab, Mitochondrial Medicine Research Centre, UMR CNRS 6015-INSERM 1083, Institut MitoVasc, University of Angers, 49933 Angers, France.
  • Chevrollier A; MitoLab, Mitochondrial Medicine Research Centre, UMR CNRS 6015-INSERM 1083, Institut MitoVasc, University of Angers, 49933 Angers, France.
  • Chaumette T; MitoLab, Mitochondrial Medicine Research Centre, UMR CNRS 6015-INSERM 1083, Institut MitoVasc, University of Angers, 49933 Angers, France.
  • Angebault C; Institut des Neurosciences de Montpellier, INSERM U1051, Université de Montpellier, France.
  • Kane S; MitoLab, Mitochondrial Medicine Research Centre, UMR CNRS 6015-INSERM 1083, Institut MitoVasc, University of Angers, 49933 Angers, France.
  • Paris A; MitoLab, Mitochondrial Medicine Research Centre, UMR CNRS 6015-INSERM 1083, Institut MitoVasc, University of Angers, 49933 Angers, France.
  • Alban J; MitoLab, Mitochondrial Medicine Research Centre, UMR CNRS 6015-INSERM 1083, Institut MitoVasc, University of Angers, 49933 Angers, France.
  • Quiles M; Institut des Neurosciences de Montpellier, INSERM U1051, Université de Montpellier, France.
  • Delettre C; Institut des Neurosciences de Montpellier, INSERM U1051, Université de Montpellier, France.
  • Bonneau D; MitoLab, Mitochondrial Medicine Research Centre, UMR CNRS 6015-INSERM 1083, Institut MitoVasc, University of Angers, 49933 Angers, France.
  • Procaccio V; MitoLab, Mitochondrial Medicine Research Centre, UMR CNRS 6015-INSERM 1083, Institut MitoVasc, University of Angers, 49933 Angers, France.
  • Amati-Bonneau P; MitoLab, Mitochondrial Medicine Research Centre, UMR CNRS 6015-INSERM 1083, Institut MitoVasc, University of Angers, 49933 Angers, France.
  • Reynier P; MitoLab, Mitochondrial Medicine Research Centre, UMR CNRS 6015-INSERM 1083, Institut MitoVasc, University of Angers, 49933 Angers, France.
  • Leruez S; MitoLab, Mitochondrial Medicine Research Centre, UMR CNRS 6015-INSERM 1083, Institut MitoVasc, University of Angers, 49933 Angers, France.
  • Calmon R; Laboratory of Genetics in Ophthalmology, INSERM UMR1163, Imagine - Institute of Genetic Diseases, Paris Descartes University, 75015 Paris, France.
  • Boddaert N; Laboratory of Genetics in Ophthalmology, INSERM UMR1163, Imagine - Institute of Genetic Diseases, Paris Descartes University, 75015 Paris, France.
  • Funalot B; Department of Genetics, IHU Necker-Enfants Malades, University Paris Descartes, 75015 Paris, France.
  • Rio M; Department of Genetics, CHU Henri Mondor, 94010 Créteil, France.
  • Bouccara D; Department of Pediatric Neurology, IHU Necker Enfants Malades and Image at Imagine, INSERM UMR1163, Imagine Institute of Genetic Diseases, Paris Descartes University, 75015 Paris, France.
  • Meunier I; Department of Genetics, IHU Necker-Enfants Malades, University Paris Descartes, 75015 Paris, France.
  • Sesaki H; Department of Genetics, CHU Henri Mondor, 94010 Créteil, France.
  • Kaplan J; Department of Pediatric Neurology, IHU Necker Enfants Malades and Image at Imagine, INSERM UMR1163, Imagine Institute of Genetic Diseases, Paris Descartes University, 75015 Paris, France.
  • Hamel CP; Service d'ORL, Hôpital Universitaire Pitié-Salpêtrière, 75013 Paris, France.
  • Rozet JM; Institut des Neurosciences de Montpellier, INSERM U1051, Université de Montpellier, France.
  • Lenaers G; Department of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Brain ; 141(4): e29, 2018 04 01.
Article in En | MEDLINE | ID: mdl-29529130
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Optic Atrophy, Autosomal Dominant / Mitochondrial Dynamics Limits: Humans Language: En Journal: Brain Year: 2018 Document type: Article Affiliation country:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Optic Atrophy, Autosomal Dominant / Mitochondrial Dynamics Limits: Humans Language: En Journal: Brain Year: 2018 Document type: Article Affiliation country: