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Genetic and Functional Analyses Point to FAN1 as the Source of Multiple Huntington Disease Modifier Effects.
Kim, Kyung-Hee; Hong, Eun Pyo; Shin, Jun Wan; Chao, Michael J; Loupe, Jacob; Gillis, Tammy; Mysore, Jayalakshmi S; Holmans, Peter; Jones, Lesley; Orth, Michael; Monckton, Darren G; Long, Jeffrey D; Kwak, Seung; Lee, Ramee; Gusella, James F; MacDonald, Marcy E; Lee, Jong-Min.
Affiliation
  • Kim KH; Molecular Neurogenetics Unit, Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA 02114, USA; Department of Neurology, Harvard Medical School, Boston, MA 02115, USA.
  • Hong EP; Molecular Neurogenetics Unit, Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA 02114, USA; Department of Neurology, Harvard Medical School, Boston, MA 02115, USA.
  • Shin JW; Molecular Neurogenetics Unit, Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA 02114, USA; Department of Neurology, Harvard Medical School, Boston, MA 02115, USA.
  • Chao MJ; Molecular Neurogenetics Unit, Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA 02114, USA; Department of Neurology, Harvard Medical School, Boston, MA 02115, USA.
  • Loupe J; Molecular Neurogenetics Unit, Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA 02114, USA; Department of Neurology, Harvard Medical School, Boston, MA 02115, USA.
  • Gillis T; Molecular Neurogenetics Unit, Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA 02114, USA.
  • Mysore JS; Molecular Neurogenetics Unit, Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA 02114, USA.
  • Holmans P; Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Department of Psychological Medicine and Neurology, School of Medicine, Cardiff University, Cardiff CF24 4HQ, UK; The GeM-HD consortium, University of Ulm, Ulm 89081, Germany.
  • Jones L; Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Department of Psychological Medicine and Neurology, School of Medicine, Cardiff University, Cardiff CF24 4HQ, UK; The GeM-HD consortium, University of Ulm, Ulm 89081, Germany.
  • Orth M; The GeM-HD consortium, University of Ulm, Ulm 89081, Germany; Department of Neurology, University of Ulm, Ulm 89081, Germany.
  • Monckton DG; The GeM-HD consortium, University of Ulm, Ulm 89081, Germany; Institute of Molecular, Cell and Systems Biology, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow G12 8QQ, UK.
  • Long JD; The GeM-HD consortium, University of Ulm, Ulm 89081, Germany; Department of Biostatistics, College of Public Health, University of Iowa, Iowa City, Iowa 52242, USA; Department of Psychiatry, Carver College of Medicine, University of Iowa, Iowa City, Iowa 52242, USA.
  • Kwak S; The GeM-HD consortium, University of Ulm, Ulm 89081, Germany; CHDI Foundation, Princeton, NJ 08540, USA.
  • Lee R; CHDI Foundation, Princeton, NJ 08540, USA.
  • Gusella JF; Molecular Neurogenetics Unit, Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA 02114, USA; The GeM-HD consortium, University of Ulm, Ulm 89081, Germany; Medical and Population Genetics Program, the Broad Institute of M.I.T. and Harvard, Cambridge, MA 02142, USA; Department of
  • MacDonald ME; Molecular Neurogenetics Unit, Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA 02114, USA; Department of Neurology, Harvard Medical School, Boston, MA 02115, USA; The GeM-HD consortium, University of Ulm, Ulm 89081, Germany; Medical and Population Genetics Program, the Broad I
  • Lee JM; Molecular Neurogenetics Unit, Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA 02114, USA; Department of Neurology, Harvard Medical School, Boston, MA 02115, USA; The GeM-HD consortium, University of Ulm, Ulm 89081, Germany; Medical and Population Genetics Program, the Broad I
Am J Hum Genet ; 107(1): 96-110, 2020 07 02.
Article in En | MEDLINE | ID: mdl-32589923
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Full text: 1 Database: MEDLINE Main subject: Huntington Disease / Endodeoxyribonucleases / Exodeoxyribonucleases / Multifunctional Enzymes Limits: Humans Language: En Year: 2020 Type: Article
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Full text: 1 Database: MEDLINE Main subject: Huntington Disease / Endodeoxyribonucleases / Exodeoxyribonucleases / Multifunctional Enzymes Limits: Humans Language: En Year: 2020 Type: Article