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The history and geographic distribution of a KCNQ1 atrial fibrillation risk allele.
Hateley, Shannon; Lopez-Izquierdo, Angelica; Jou, Chuanchau J; Cho, Scott; Schraiber, Joshua G; Song, Shiya; Maguire, Colin T; Torres, Natalia; Riedel, Michael; Bowles, Neil E; Arrington, Cammon B; Kennedy, Brett J; Etheridge, Susan P; Lai, Shuping; Pribble, Chase; Meyers, Lindsay; Lundahl, Derek; Byrnes, Jake; Granka, Julie M; Kauffman, Christopher A; Lemmon, Gordon; Boyden, Steven; Scott Watkins, W; Karren, Mary Anne; Knight, Stacey; Brent Muhlestein, J; Carlquist, John F; Anderson, Jeffrey L; Chahine, Kenneth G; Shah, Khushi U; Ball, Catherine A; Benjamin, Ivor J; Yandell, Mark; Tristani-Firouzi, Martin.
Afiliação
  • Hateley S; AncestryDNA, San Francisco, CA, USA.
  • Lopez-Izquierdo A; Nora Eccles Harrison CVRTI, University of Utah School of Medicine, Salt Lake City, UT, USA.
  • Jou CJ; Nora Eccles Harrison CVRTI, University of Utah School of Medicine, Salt Lake City, UT, USA.
  • Cho S; Division of Pediatric Cardiology, University of Utah School of Medicine, Salt Lake City, UT, USA.
  • Schraiber JG; Nora Eccles Harrison CVRTI, University of Utah School of Medicine, Salt Lake City, UT, USA.
  • Song S; AncestryDNA, San Francisco, CA, USA.
  • Maguire CT; AncestryDNA, San Francisco, CA, USA.
  • Torres N; Nora Eccles Harrison CVRTI, University of Utah School of Medicine, Salt Lake City, UT, USA.
  • Riedel M; Nora Eccles Harrison CVRTI, University of Utah School of Medicine, Salt Lake City, UT, USA.
  • Bowles NE; Cardiovascular Center, Medical College of Wisconsin, Milwaukee, WI, USA.
  • Arrington CB; Division of Pediatric Cardiology, University of Utah School of Medicine, Salt Lake City, UT, USA.
  • Kennedy BJ; Division of Pediatric Cardiology, University of Utah School of Medicine, Salt Lake City, UT, USA.
  • Etheridge SP; Department of Human Genetics, University of Utah, Salt Lake City, UT, USA.
  • Lai S; Division of Pediatric Cardiology, University of Utah School of Medicine, Salt Lake City, UT, USA.
  • Pribble C; Cardiovascular Center, Medical College of Wisconsin, Milwaukee, WI, USA.
  • Meyers L; Nora Eccles Harrison CVRTI, University of Utah School of Medicine, Salt Lake City, UT, USA.
  • Lundahl D; Division of Pediatric Cardiology, University of Utah School of Medicine, Salt Lake City, UT, USA.
  • Byrnes J; Division of Pediatric Cardiology, University of Utah School of Medicine, Salt Lake City, UT, USA.
  • Granka JM; AncestryDNA, San Francisco, CA, USA.
  • Kauffman CA; AncestryDNA, San Francisco, CA, USA.
  • Lemmon G; Nora Eccles Harrison CVRTI, University of Utah School of Medicine, Salt Lake City, UT, USA.
  • Boyden S; Department of Human Genetics, University of Utah, Salt Lake City, UT, USA.
  • Scott Watkins W; Department of Human Genetics, University of Utah, Salt Lake City, UT, USA.
  • Karren MA; Department of Human Genetics, University of Utah, Salt Lake City, UT, USA.
  • Knight S; Department of Human Genetics, University of Utah, Salt Lake City, UT, USA.
  • Brent Muhlestein J; The Intermountain Medical Center, Murray, UT, USA.
  • Carlquist JF; The Intermountain Medical Center, Murray, UT, USA.
  • Anderson JL; The Intermountain Medical Center, Murray, UT, USA.
  • Chahine KG; The Intermountain Medical Center, Murray, UT, USA.
  • Shah KU; AncestryDNA, San Francisco, CA, USA.
  • Ball CA; Nora Eccles Harrison CVRTI, University of Utah School of Medicine, Salt Lake City, UT, USA.
  • Benjamin IJ; AncestryDNA, San Francisco, CA, USA.
  • Yandell M; Cardiovascular Center, Medical College of Wisconsin, Milwaukee, WI, USA.
  • Tristani-Firouzi M; Department of Human Genetics, University of Utah, Salt Lake City, UT, USA.
Nat Commun ; 12(1): 6442, 2021 11 08.
Article em En | MEDLINE | ID: mdl-34750360

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fibrilação Atrial / Predisposição Genética para Doença / Mutação de Sentido Incorreto / Polimorfismo de Nucleotídeo Único / Canal de Potássio KCNQ1 Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged País/Região como assunto: America do norte / Europa Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fibrilação Atrial / Predisposição Genética para Doença / Mutação de Sentido Incorreto / Polimorfismo de Nucleotídeo Único / Canal de Potássio KCNQ1 Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged País/Região como assunto: America do norte / Europa Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos