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Asymmetry of parental origin in long QT syndrome: preferential maternal transmission of KCNQ1 variants linked to channel dysfunction.
Itoh, Hideki; Berthet, Myriam; Fressart, Véronique; Denjoy, Isabelle; Maugenre, Svetlana; Klug, Didier; Mizusawa, Yuka; Makiyama, Takeru; Hofman, Nynke; Stallmeyer, Birgit; Zumhagen, Sven; Shimizu, Wataru; Wilde, Arthur A M; Schulze-Bahr, Eric; Horie, Minoru; Tezenas du Montcel, Sophie; Guicheney, Pascale.
Afiliação
  • Itoh H; INSERM, UMR S1166, Paris, France.
  • Berthet M; Sorbonne Universités, UPMC Univ Paris 06, UMR S1166, Paris, France.
  • Fressart V; Department of Cardiovascular and Respiratory Medicine, Shiga University of Medical Science, Otsu, Japan.
  • Denjoy I; INSERM, UMR S1166, Paris, France.
  • Maugenre S; Sorbonne Universités, UPMC Univ Paris 06, UMR S1166, Paris, France.
  • Klug D; Institute of Cardiometabolism and Nutrition, ICAN, Pitié-Salpêtrière Hospital, Paris, France.
  • Mizusawa Y; INSERM, UMR S1166, Paris, France.
  • Makiyama T; Sorbonne Universités, UPMC Univ Paris 06, UMR S1166, Paris, France.
  • Hofman N; Institute of Cardiometabolism and Nutrition, ICAN, Pitié-Salpêtrière Hospital, Paris, France.
  • Stallmeyer B; AP-HP, Groupe Hospitalier Pitié-Salpétrière, Service de Biochimie Métabolique, UF Cardiogénétique et Myogénétique Moléculaire et Cellulaire, Paris, France.
  • Zumhagen S; INSERM, UMR S1166, Paris, France.
  • Shimizu W; Cardiology Department, AP-HP, Hôpital Bichat, Paris, France.
  • Wilde AA; INSERM, UMR S1166, Paris, France.
  • Schulze-Bahr E; Sorbonne Universités, UPMC Univ Paris 06, UMR S1166, Paris, France.
  • Horie M; Institute of Cardiometabolism and Nutrition, ICAN, Pitié-Salpêtrière Hospital, Paris, France.
  • Tezenas du Montcel S; Hôpital Cardiologique de Lille, CHRU, Service de cardiologie A, Lille, France.
  • Guicheney P; AMC Heart Center, Department of Clinical and Experimental Cardiology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Eur J Hum Genet ; 24(8): 1160-6, 2016 08.
Article em En | MEDLINE | ID: mdl-26669661
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome do QT Longo / Canal de Potássio KCNQ1 / Herança Paterna / Mutação Limite: Adult / Child / Female / Humans / Male Idioma: En Revista: Eur J Hum Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: França
Texto completo
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PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome do QT Longo / Canal de Potássio KCNQ1 / Herança Paterna / Mutação Limite: Adult / Child / Female / Humans / Male Idioma: En Revista: Eur J Hum Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: França