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Early somatic mosaicism is a rare cause of long-QT syndrome.
Priest, James Rush; Gawad, Charles; Kahlig, Kristopher M; Yu, Joseph K; O'Hara, Thomas; Boyle, Patrick M; Rajamani, Sridharan; Clark, Michael J; Garcia, Sarah T K; Ceresnak, Scott; Harris, Jason; Boyle, Sean; Dewey, Frederick E; Malloy-Walton, Lindsey; Dunn, Kyla; Grove, Megan; Perez, Marco V; Neff, Norma F; Chen, Richard; Maeda, Katsuhide; Dubin, Anne; Belardinelli, Luiz; West, John; Antolik, Christian; Macaya, Daniela; Quertermous, Thomas; Trayanova, Natalia A; Quake, Stephen R; Ashley, Euan A.
Afiliación
  • Priest JR; Stanford Center for Inherited Cardiovascular Disease, Stanford University School of Medicine, Stanford, CA 94305; Child Health Research Institute, Stanford University School of Medicine, Stanford, CA 94305; Division of Pediatric Cardiology, Stanford University School of Medicine, Stanford, CA 94305.
  • Gawad C; Child Health Research Institute, Stanford University School of Medicine, Stanford, CA 94305; Division of Pediatric Hematology-Oncology, Stanford University School of Medicine, Stanford, CA 94305.
  • Kahlig KM; Department of Biology, Cardiovascular Therapeutic Area, Gilead Sciences, Fremont, CA 94555.
  • Yu JK; Department of Biomedical Engineering, Johns Hopkins University, Baltimore, MD 21218; Institute for Computational Medicine, Johns Hopkins University, Baltimore, MD 21218.
  • O'Hara T; Department of Biomedical Engineering, Johns Hopkins University, Baltimore, MD 21218.
  • Boyle PM; Department of Biomedical Engineering, Johns Hopkins University, Baltimore, MD 21218; Institute for Computational Medicine, Johns Hopkins University, Baltimore, MD 21218.
  • Rajamani S; Department of Biology, Cardiovascular Therapeutic Area, Gilead Sciences, Fremont, CA 94555.
  • Clark MJ; Personalis, Inc., Menlo Park, CA 94025.
  • Garcia ST; Personalis, Inc., Menlo Park, CA 94025.
  • Ceresnak S; Stanford Center for Inherited Cardiovascular Disease, Stanford University School of Medicine, Stanford, CA 94305; Child Health Research Institute, Stanford University School of Medicine, Stanford, CA 94305; Division of Pediatric Cardiology, Stanford University School of Medicine, Stanford, CA 94305.
  • Harris J; Personalis, Inc., Menlo Park, CA 94025.
  • Boyle S; Personalis, Inc., Menlo Park, CA 94025.
  • Dewey FE; Stanford Center for Inherited Cardiovascular Disease, Stanford University School of Medicine, Stanford, CA 94305; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA 94305.
  • Malloy-Walton L; Stanford Center for Inherited Cardiovascular Disease, Stanford University School of Medicine, Stanford, CA 94305; Child Health Research Institute, Stanford University School of Medicine, Stanford, CA 94305; Division of Pediatric Cardiology, Stanford University School of Medicine, Stanford, CA 94305.
  • Dunn K; Stanford Center for Inherited Cardiovascular Disease, Stanford University School of Medicine, Stanford, CA 94305; Lucile Packard Children's Hospital Heart Center, Palo Alto, CA 94304.
  • Grove M; Stanford Center for Inherited Cardiovascular Disease, Stanford University School of Medicine, Stanford, CA 94305; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA 94305.
  • Perez MV; Stanford Center for Inherited Cardiovascular Disease, Stanford University School of Medicine, Stanford, CA 94305; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA 94305.
  • Neff NF; Department of Bioengineering, Stanford University School of Medicine, Stanford, CA 94305.
  • Chen R; Personalis, Inc., Menlo Park, CA 94025.
  • Maeda K; Stanford Center for Inherited Cardiovascular Disease, Stanford University School of Medicine, Stanford, CA 94305; Division of Cardiothoracic Surgery, Stanford University School of Medicine, Stanford, CA 94305.
  • Dubin A; Stanford Center for Inherited Cardiovascular Disease, Stanford University School of Medicine, Stanford, CA 94305; Child Health Research Institute, Stanford University School of Medicine, Stanford, CA 94305; Division of Pediatric Cardiology, Stanford University School of Medicine, Stanford, CA 94305.
  • Belardinelli L; Department of Biology, Cardiovascular Therapeutic Area, Gilead Sciences, Fremont, CA 94555.
  • West J; Personalis, Inc., Menlo Park, CA 94025.
  • Antolik C; Cardiogenetic Testing Services, GeneDx, Gaithersburg, MD 20877.
  • Macaya D; Cardiogenetic Testing Services, GeneDx, Gaithersburg, MD 20877.
  • Quertermous T; Stanford Center for Inherited Cardiovascular Disease, Stanford University School of Medicine, Stanford, CA 94305; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA 94305.
  • Trayanova NA; Department of Biomedical Engineering, Johns Hopkins University, Baltimore, MD 21218; Institute for Computational Medicine, Johns Hopkins University, Baltimore, MD 21218.
  • Quake SR; Department of Bioengineering, Stanford University School of Medicine, Stanford, CA 94305; Department of Applied Physics, Stanford University, Stanford, CA 94305; Howard Hughes Medical Research Institute, Stanford University School of Medicine, Stanford, CA 94305 euan@stanford.edu quake@stanford.edu.
  • Ashley EA; Stanford Center for Inherited Cardiovascular Disease, Stanford University School of Medicine, Stanford, CA 94305; Child Health Research Institute, Stanford University School of Medicine, Stanford, CA 94305; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA 943
Proc Natl Acad Sci U S A ; 113(41): 11555-11560, 2016 10 11.
Article en En | MEDLINE | ID: mdl-27681629
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndrome de QT Prolongado / Predisposición Genética a la Enfermedad / Mosaicismo Tipo de estudio: Prognostic_studies Límite: Humans / Infant Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2016 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndrome de QT Prolongado / Predisposición Genética a la Enfermedad / Mosaicismo Tipo de estudio: Prognostic_studies Límite: Humans / Infant Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2016 Tipo del documento: Article