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Genetic causes of rare and common epilepsies: What should the epileptologist know?
Lesca, Gaetan; Baumgartner, Tobias; Monin, Pauline; De Dominicis, Angela; Kunz, Wolfram S; Specchio, Nicola.
Afiliação
  • Lesca G; Department of Medical Genetics and Department of Paedaitric Clinical Epileptology, Member of the ERN EpiCARE, University Hospitals of Lyon (HCL), Lyon, France; University Claude Bernard Lyon 1, Lyon, France. Electronic address: gaetan.lesca@chu-lyon.fr.
  • Baumgartner T; Department of Epileptology, University Hospital Bonn, Member of the ERN EpiCARE, Bonn, Germany.
  • Monin P; Department of Medical Genetics and Department of Paedaitric Clinical Epileptology, Member of the ERN EpiCARE, University Hospitals of Lyon (HCL), Lyon, France; University Claude Bernard Lyon 1, Lyon, France.
  • De Dominicis A; Laboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesù Children Hospital, IRCCS, Rome, Italy.
  • Kunz WS; Department of Epileptology, University Hospital Bonn, Member of the ERN EpiCARE, Bonn, Germany.
  • Specchio N; Rare and Complex Epilepsy Unit, Department of Neuroscience, Bambino Gesù Children's Hospital, IRCCS, Full Member of European Reference Network EpiCARE, Rome, Italy.
Eur J Med Genet ; 65(9): 104570, 2022 Sep.
Article em En | MEDLINE | ID: mdl-35850153
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Testes Genéticos / Epilepsia Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies Limite: Humans Idioma: En Revista: Eur J Med Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Testes Genéticos / Epilepsia Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies Limite: Humans Idioma: En Revista: Eur J Med Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2022 Tipo de documento: Article