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Correction to: Myoclonic status epilepticus and cerebellar hypoplasia associated with a novel variant in the GRIA3 gene.
Rinaldi, Berardo; Ge, Yu-Han; Freri, Elena; Tucci, Arianna; Granata, Tiziana; Estienne, Margherita; Sun, Jia-Hui; Gérard, Bénédicte; Bayat, Allan; Efthymiou, Stephanie; Gervasini, Cristina; Shi, Yun Stone; Houlden, Henry; Marchisio, Paola; Milani, Donatella.
Afiliação
  • Rinaldi B; Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
  • Ge YH; Ministry of Education Key Laboratory of Model Animal for Disease Study, Department of Neurology, Drum Tower Hospital, Medical School, Nanjing University, Nanjing, China.
  • Freri E; State Key Laboratory of Pharmaceutical Biotechnology, Model Animal Research Center, Institute for Brain Sciences, Chemistry and Biomedicine Innovation Center, Nanjing University, Nanjing, China.
  • Tucci A; Department of Pediatric Neuroscience, Fondazione IRCCS Istituto Neurologico C. Besta, Milan, Italy.
  • Granata T; Clinical Pharmacology, William Harvey Research Institute, School of Medicine and Dentistry, Queen Mary University of London, London, EC1M 6BQ, UK. a.tucci@qmul.ac.uk.
  • Estienne M; Department of Pediatric Neuroscience, Fondazione IRCCS Istituto Neurologico C. Besta, Milan, Italy.
  • Sun JH; Department of Pediatric Neuroscience, Fondazione IRCCS Istituto Neurologico C. Besta, Milan, Italy.
  • Gérard B; Ministry of Education Key Laboratory of Model Animal for Disease Study, Department of Neurology, Drum Tower Hospital, Medical School, Nanjing University, Nanjing, China.
  • Bayat A; State Key Laboratory of Pharmaceutical Biotechnology, Model Animal Research Center, Institute for Brain Sciences, Chemistry and Biomedicine Innovation Center, Nanjing University, Nanjing, China.
  • Efthymiou S; Laboratoires de diagnostic génétique, Institut Medical d'Alsace, Hôpitaux Universitaire de Strasbourg, Strasbourg, France.
  • Gervasini C; Department for Genetics and Personalized Medicine, Danish Epilepsy Centre, Dianalund, Denmark.
  • Shi YS; Institute for Regional Health Services Research, University of Southern Denmark, Odense, Denmark.
  • Houlden H; Department of Neuromuscular disorders, UCL Queen Square Institute of Neurology, London, UK.
  • Marchisio P; Medical Genetics, Department of Health Sciences, Università degli Studi di Milano, Milan, Italy.
  • Milani D; Ministry of Education Key Laboratory of Model Animal for Disease Study, Department of Neurology, Drum Tower Hospital, Medical School, Nanjing University, Nanjing, China. yunshi@nju.edu.cn.
Neurogenetics ; 23(1): 81, 2022 Jan.
Article em En | MEDLINE | ID: mdl-34837146
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: Neurogenetics Assunto da revista: GENETICA / NEUROLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Itália
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: Neurogenetics Assunto da revista: GENETICA / NEUROLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Itália