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Mutación en el gen KCNQ1 y epilepsia en paciente con síndrome de QT largo / KCNQ1 gene mutation and epilepsy in patient with long QT syndrome
García Gozalo, Macarena; Bermejo Arnedo, Ignacio; de Vera McMullan, Paula.
Affiliation
  • García Gozalo, Macarena; Hospital Universitario Infanta Cristina. Parla. España
  • Bermejo Arnedo, Ignacio; Hospital Universitario Infanta Cristina. Parla. España
  • de Vera McMullan, Paula; Hospital Universitario Infanta Cristina. Parla. España
Med. clín (Ed. impr.) ; 157(9): 456-457, noviembre 2021.
Article in Spanish | IBECS | ID: ibc-215656
Responsible library: ES1.1
Localization: ES15.1 - BNCS
Subject(s)
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Collection: National databases / Spain Database: IBECS Main subject: Long QT Syndrome / Epilepsy / KCNQ1 Potassium Channel / Mutation Limits: Child, preschool / Female / Humans Language: Spanish Journal: Med. clín (Ed. impr.) Year: 2021 Document type: Article Institution/Affiliation country: Hospital Universitario Infanta Cristina/España
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Collection: National databases / Spain Database: IBECS Main subject: Long QT Syndrome / Epilepsy / KCNQ1 Potassium Channel / Mutation Limits: Child, preschool / Female / Humans Language: Spanish Journal: Med. clín (Ed. impr.) Year: 2021 Document type: Article Institution/Affiliation country: Hospital Universitario Infanta Cristina/España