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Wolff-Parkinson-White syndrome: De novo variants and evidence for mutational burden in genes associated with atrial fibrillation.
Coban-Akdemir, Zeynep H; Charng, Wu-Lin; Azamian, Mahshid; Paine, Ingrid S; Punetha, Jaya; Grochowski, Christopher M; Gambin, Tomasz; Valdes, Santiago O; Cannon, Bryan; Zapata, Gladys; Hernandez, Patricia P; Jhangiani, Shalini; Doddapaneni, Harsha; Hu, Jianhong; Boricha, Fatima; Muzny, Donna M; Boerwinkle, Eric; Yang, Yaping; Gibbs, Richard A; Posey, Jennifer E; Wehrens, Xander H T; Belmont, John W; Kim, Jeffrey J; Miyake, Christina Y; Lupski, James R; Lalani, Seema R.
Afiliação
  • Coban-Akdemir ZH; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
  • Charng WL; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
  • Azamian M; Current affiliation: Department of Neurology, Washington University School of Medicine, St. Louis, Missouri, USA.
  • Paine IS; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
  • Punetha J; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
  • Grochowski CM; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
  • Gambin T; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
  • Valdes SO; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
  • Cannon B; Current affiliation: Institute of Computer Science, Warsaw University of Technology, Warsaw, Poland.
  • Zapata G; Department of Pediatrics, Division of Cardiology, Texas Children's Hospital, Houston, Texas, USA.
  • Hernandez PP; Department of Cardiovascular Diseases, Mayo Clinic, Rochester, Minnesota, USA.
  • Jhangiani S; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
  • Doddapaneni H; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
  • Hu J; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
  • Boricha F; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, USA.
  • Muzny DM; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, USA.
  • Boerwinkle E; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, USA.
  • Yang Y; Department of Pediatrics, the University of Texas Health Science Center at Houston, Houston, Texas, USA.
  • Gibbs RA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
  • Posey JE; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, USA.
  • Wehrens XHT; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, USA.
  • Belmont JW; Human Genetics Center, The University of Texas Health Science Center at Houston, Houston, Texas, USA.
  • Kim JJ; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
  • Miyake CY; Baylor Genetics Laboratories, Baylor College of Medicine, Houston, Texas, USA.
  • Lupski JR; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
  • Lalani SR; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, USA.
Am J Med Genet A ; 182(6): 1387-1399, 2020 06.
Article em En | MEDLINE | ID: mdl-32233023
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fibrilação Atrial / Síndrome de Wolff-Parkinson-White / Predisposição Genética para Doença / Proteínas Quinases Ativadas por AMP Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fibrilação Atrial / Síndrome de Wolff-Parkinson-White / Predisposição Genética para Doença / Proteínas Quinases Ativadas por AMP Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article