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Whole-Exome Sequencing in Familial Parkinson Disease.
Farlow, Janice L; Robak, Laurie A; Hetrick, Kurt; Bowling, Kevin; Boerwinkle, Eric; Coban-Akdemir, Zeynep H; Gambin, Tomasz; Gibbs, Richard A; Gu, Shen; Jain, Preti; Jankovic, Joseph; Jhangiani, Shalini; Kaw, Kaveeta; Lai, Dongbing; Lin, Hai; Ling, Hua; Liu, Yunlong; Lupski, James R; Muzny, Donna; Porter, Paula; Pugh, Elizabeth; White, Janson; Doheny, Kimberly; Myers, Richard M; Shulman, Joshua M; Foroud, Tatiana.
Afiliación
  • Farlow JL; Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis.
  • Robak LA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas3Department of Pediatrics, Baylor College of Medicine, Houston, Texas4Department of Pediatrics, Texas Children's Hospital, Houston5Jan and Dan Duncan Neurological Resear.
  • Hetrick K; Center for Inherited Disease Research, The Johns Hopkins University, Baltimore, Maryland.
  • Bowling K; HudsonAlpha Institute for Biotechnology, Huntsville, Alabama.
  • Boerwinkle E; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas9Human Genetics Center, University of Texas Health Science Center, Houston.
  • Coban-Akdemir ZH; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
  • Gambin T; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
  • Gibbs RA; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas.
  • Gu S; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
  • Jain P; HudsonAlpha Institute for Biotechnology, Huntsville, Alabama10Department of Pediatrics, Columbia University Medical Center, New York, New York.
  • Jankovic J; Department of Neurology, Baylor College of Medicine, Houston, Texas.
  • Jhangiani S; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas.
  • Kaw K; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas5Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston.
  • Lai D; Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis.
  • Lin H; Department of BioHealth Informatics, Indiana University School of Informatics and Computing, Indianapolis.
  • Ling H; Center for Inherited Disease Research, The Johns Hopkins University, Baltimore, Maryland.
  • Liu Y; Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis.
  • Lupski JR; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas3Department of Pediatrics, Baylor College of Medicine, Houston, Texas4Department of Pediatrics, Texas Children's Hospital, Houston8Human Genome Sequencing Center, Baylor.
  • Muzny D; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas.
  • Porter P; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas5Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston.
  • Pugh E; Center for Inherited Disease Research, The Johns Hopkins University, Baltimore, Maryland.
  • White J; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
  • Doheny K; Center for Inherited Disease Research, The Johns Hopkins University, Baltimore, Maryland.
  • Myers RM; HudsonAlpha Institute for Biotechnology, Huntsville, Alabama.
  • Shulman JM; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas5Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston11Department of Neurology, Baylor College of Medicine, Houston, Texas13Department.
  • Foroud T; Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis.
JAMA Neurol ; 73(1): 68-75, 2016 Jan.
Article en En | MEDLINE | ID: mdl-26595808
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas Tirosina Quinasas / Análisis de Secuencia de ADN / Tenascina / Trastornos Parkinsonianos / Exoma Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: JAMA Neurol Año: 2016 Tipo del documento: Article Pais de publicación: Estados Unidos
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas Tirosina Quinasas / Análisis de Secuencia de ADN / Tenascina / Trastornos Parkinsonianos / Exoma Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: JAMA Neurol Año: 2016 Tipo del documento: Article Pais de publicación: Estados Unidos