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A KCNC1 mutation in epilepsy of infancy with focal migrating seizures produces functional channels that fail to be regulated by PKC phosphorylation.
Zhang, Yalan; Ali, Syed R; Nabbout, Rima; Barcia, Giulia; Kaczmarek, Leonard K.
Afiliación
  • Zhang Y; Department of Pharmacology, Yale University School of Medicine, New Haven, Connecticut.
  • Ali SR; Department of Pharmacology, Yale University School of Medicine, New Haven, Connecticut.
  • Nabbout R; Department of Pediatric Neurology, Necker-Enfants Malades Hospital, Centre de Référence Épilepsies Rares, Member of ERN EPICARE, Institut Imagine, Université de Paris, Paris, France.
  • Barcia G; Department of Pediatric Neurology, Necker-Enfants Malades Hospital, Centre de Référence Épilepsies Rares, Member of ERN EPICARE, Institut Imagine, Université de Paris, Paris, France.
  • Kaczmarek LK; Department of Medical Genetics, Necker-Enfants Malades Hospital, Université de Paris, Paris, France.
J Neurophysiol ; 126(2): 532-539, 2021 08 01.
Article en En | MEDLINE | ID: mdl-34232791
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Sialiltransferasas / Epilepsia / Canales de Potasio Shaw / Mutación Límite: Animals Idioma: En Revista: J Neurophysiol Año: 2021 Tipo del documento: Article
Texto completo
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XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Sialiltransferasas / Epilepsia / Canales de Potasio Shaw / Mutación Límite: Animals Idioma: En Revista: J Neurophysiol Año: 2021 Tipo del documento: Article