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TBX5-encoded T-box transcription factor 5 variant T223M is associated with long QT syndrome and pediatric sudden cardiac death.
Markunas, Alexandra M; Manivannan, Perathu K R; Ezekian, Jordan E; Agarwal, Agnim; Eisner, William; Alsina, Katherina; Allen, Hugh D; Wray, Gregory A; Kim, Jeffrey J; Wehrens, Xander H T; Landstrom, Andrew P.
Afiliação
  • Markunas AM; Department of Pediatrics, Division of Cardiology, Duke University School of Medicine, Durham, North Carolina, USA.
  • Manivannan PKR; Department of Pediatrics, Division of Cardiology, Duke University School of Medicine, Durham, North Carolina, USA.
  • Ezekian JE; Department of Pediatrics, Division of Cardiology, Duke University School of Medicine, Durham, North Carolina, USA.
  • Agarwal A; Department of Biology, Duke University, Durham, North Carolina, USA.
  • Eisner W; Department of Pediatrics, Division of Cardiology, Duke University School of Medicine, Durham, North Carolina, USA.
  • Alsina K; Departments of Molecular Physiology & Biophysics and Medicine (Cardiology), Baylor College of Medicine, Houston, Texas, USA.
  • Allen HD; Department of Pediatrics, Section of Cardiology, Baylor College of Medicine, Houston, Texas, USA.
  • Wray GA; Department of Biology, Duke University, Durham, North Carolina, USA.
  • Kim JJ; Department of Pediatrics, Section of Cardiology, Baylor College of Medicine, Houston, Texas, USA.
  • Wehrens XHT; Departments of Molecular Physiology & Biophysics and Medicine (Cardiology), Baylor College of Medicine, Houston, Texas, USA.
  • Landstrom AP; Department of Pediatrics, Division of Cardiology, Duke University School of Medicine, Durham, North Carolina, USA.
Am J Med Genet A ; 185(3): 923-929, 2021 03.
Article em En | MEDLINE | ID: mdl-33369127
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome do QT Longo / Morte Súbita Cardíaca / Mutação Puntual / Mutação de Sentido Incorreto / Proteínas com Domínio T Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome do QT Longo / Morte Súbita Cardíaca / Mutação Puntual / Mutação de Sentido Incorreto / Proteínas com Domínio T Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos