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Wolff–Parkinson–White syndrome: De novo variants and evidence for mutational burden in genes associated with atrial fibrillation
Authors:Zeynep H Coban‐Akdemir  Wu‐Lin Charng  Mahshid Azamian  Ingrid S Paine  Jaya Punetha  Christopher M Grochowski  Tomasz Gambin  Santiago O Valdes  Bryan Cannon  Gladys Zapata  Patricia P Hernandez  Shalini Jhangiani  Harsha Doddapaneni  Jianhong Hu  Fatima Boricha  Donna M Muzny  Eric Boerwinkle  Yaping Yang  Richard A Gibbs  Jennifer E Posey  Xander H T Wehrens  John W Belmont  Jeffrey J Kim  Christina Y Miyake  James R Lupski  Seema R Lalani
Institution:1. Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA;2. Current affiliation: Department of Neurology, Washington University School of Medicine, St. Louis, Missouri, USA;3. Current affiliation: Institute of Computer Science, Warsaw University of Technology, Warsaw, Poland;4. Department of Pediatrics, Division of Cardiology, Texas Children's Hospital, Houston, Texas, USA;5. Department of Cardiovascular Diseases, Mayo Clinic, Rochester, Minnesota, USA;6. Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, USA;7. Department of Pediatrics, the University of Texas Health Science Center at Houston, Houston, Texas, USA;8. Human Genetics Center, The University of Texas Health Science Center at Houston, Houston, Texas, USA;9. Baylor Genetics Laboratories, Baylor College of Medicine, Houston, Texas, USA;10. Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, Texas, USA;11. Cardiovascular Research Institute, Baylor College of Medicine, Houston, Texas, USA;12. Department of Pediatrics, Texas Children's Hospital, Houston, Texas, USA;13. Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA;14. Texas Children's Hospital, Houston, Texas, USA;15.
Abstract:
Keywords:   ANK2  atrial fibrillation  exome sequencing  Wolff–  Parkinson–  White (WPW) syndrome
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