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A Dominant Mutation in FBXO38 Causes Distal Spinal Muscular Atrophy with Calf Predominance
Authors:Charlotte J Sumner  Constantin d’Ydewalle  Joe Wooley  Katherine A Fawcett  Dena Hernandez  Alice R Gardiner  Bernadett Kalmar  Robert H Baloh  Michael Gonzalez  Stephan Züchner  Horia C Stanescu  Robert Kleta  Ami Mankodi  David R Cornblath  Kevin B Boylan  Mary M Reilly  Linda Greensmith  Andrew B Singleton  Matthew B Harms  Alexander M Rossor  Henry Houlden
Institution:1 Department of Neurology, Johns Hopkins School of Medicine, Baltimore, MD 21205, USA;2 Department of Neuroscience, Johns Hopkins School of Medicine, Baltimore, MD 21205, USA;3 Laboratory for Neurobiology, Vesalius Research Center, VIB and KU Leuven, 3000 Leuven, Belgium;4 Department of Molecular Neuroscience, The National Hospital for Neurology and Neurosurgery and UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK;5 The MRC Centre for Neuromuscular Diseases, The National Hospital for Neurology and Neurosurgery and UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK;6 Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD 20892, USA;7 Department of Neurology, Cedars-Sinai Medical Center, Los Angeles, CA 90095, USA;8 Dr. John T. MacDonald Department of Human Genetics and Hussman Institute for Human Genomics, Miller School of Medicine, University of Miami, FL 33136, USA;9 Center for Nephrology, University College London, London WC1N 3BG, UK;10 Neurogenetics Branch, National Institute of Neurological Disorders and Stroke, Bethesda, MD 20892, USA;11 Department of Neurology, Mayo Clinic, Jacksonville, FL 32224, USA;12 Department of Neurology, Washington University School of Medicine, St. Louis, MO 63110, USA
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