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KCNQ2 Mutation Explains the Etiology of Chloral Hydrate-Responsive Ohtahara Syndrome.
Sterbová, Katalin; Lassuthová, Petra; Perníková, Ivana; Beran, Michal; Neupauerová, Jana; Krsek, Pavel; Seeman, Pavel.
Afiliação
  • Sterbová K; Department of Child Neurology, 2nd Faculty of Medicine, Charles University and Motol Hospital, Prague, Czech Republic.
  • Lassuthová P; DNA Laboratory, Department of Child Neurology, 2nd Faculty of Medicine, Charles University and Motol Hospital, Prague, Czech Republic. Electronic address: petra.lassuthova@gmail.com.
  • Perníková I; Department of Child Neurology, 2nd Faculty of Medicine, Charles University and Motol Hospital, Prague, Czech Republic.
  • Beran M; Department of Forensic Medicine, Bulovka Hospital, Prague, Czech Republic.
  • Neupauerová J; DNA Laboratory, Department of Child Neurology, 2nd Faculty of Medicine, Charles University and Motol Hospital, Prague, Czech Republic.
  • Krsek P; Department of Child Neurology, 2nd Faculty of Medicine, Charles University and Motol Hospital, Prague, Czech Republic.
  • Seeman P; DNA Laboratory, Department of Child Neurology, 2nd Faculty of Medicine, Charles University and Motol Hospital, Prague, Czech Republic.
Pediatr Neurol ; 67: e3-e4, 2017 02.
Article em En | MEDLINE | ID: mdl-28065823
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Espasmos Infantis / Hidrato de Cloral / Canal de Potássio KCNQ2 / Hipnóticos e Sedativos Idioma: En Ano de publicação: 2017 Tipo de documento: Article País de afiliação: República Tcheca
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Espasmos Infantis / Hidrato de Cloral / Canal de Potássio KCNQ2 / Hipnóticos e Sedativos Idioma: En Ano de publicação: 2017 Tipo de documento: Article País de afiliação: República Tcheca