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A trafficking-deficient KCNQ1 mutation, T587M, causes a severe phenotype of long QT syndrome by interfering with intracellular hERG transport.
Wu, Jie; Sakaguchi, Tomoko; Takenaka, Kotoe; Toyoda, Futoshi; Tsuji, Keiko; Matsuura, Hiroshi; Horie, Minoru.
Afiliação
  • Wu J; Department of Pharmacology, School of Basic Medical Science, Xi'an Jiaotong University Health Science Center, Xi'an, Shaanxi, China; Department of Cardiovascular and Respiratory Medicine, Shiga University of Medical Science, Otsu, Japan; Department of Physiology, Shiga University of Medical Science,
  • Sakaguchi T; Department of Cardiovascular and Respiratory Medicine, Shiga University of Medical Science, Otsu, Japan.
  • Takenaka K; Department of Cardiovascular Medicine, Kyoto University Graduate School of Medicine, Kyoto, Japan.
  • Toyoda F; Department of Physiology, Shiga University of Medical Science, Otsu, Japan.
  • Tsuji K; Department of Cardiovascular and Respiratory Medicine, Shiga University of Medical Science, Otsu, Japan.
  • Matsuura H; Department of Physiology, Shiga University of Medical Science, Otsu, Japan.
  • Horie M; Department of Cardiovascular and Respiratory Medicine, Shiga University of Medical Science, Otsu, Japan. Electronic address: livedoor629@gmail.com.
J Cardiol ; 73(5): 343-350, 2019 05.
Article em En | MEDLINE | ID: mdl-30591322

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Síndrome do QT Longo / Canal de Potássio KCNQ1 / Canais de Potássio Éter-A-Go-Go Tipo de estudo: Etiology_studies Limite: Humans Idioma: En Revista: J Cardiol Assunto da revista: CARDIOLOGIA Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Síndrome do QT Longo / Canal de Potássio KCNQ1 / Canais de Potássio Éter-A-Go-Go Tipo de estudo: Etiology_studies Limite: Humans Idioma: En Revista: J Cardiol Assunto da revista: CARDIOLOGIA Ano de publicação: 2019 Tipo de documento: Article