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Duchenne/Becker muscular dystrophy: correlation of phenotype by electroretinography with sites of dystrophin mutations
Authors:De-Ann M Pillers  KM Fitzgerald  NM Duncan  SM Rash  RA White  SJ Dwinnell  BR Powell  RE Schnur  PN Ray  GW Cibis  RG Weleber
Institution:(1) Department of Pediatrics, NRC-5, Oregon Child Health Research Center, Doernbecher Children's Hospital, Oregon Health Sciences University, 3181 SW Sam Jackson Park Rd., Portland, OR 97201–3042, USA,;(2) Department of Molecular and Medical Genetics, Oregon Health Sciences University, Portland, Ore., USA,;(3) Department of Ophthalmology, The Casey Eye Institute, Oregon Health Sciences University, Portland, Ore., USA,;(4) Section of Genetics, University of Missouri School of Medicine, Kansas City, Mo., USA,;(5) Section of Ophthalmology, University of Missouri School of Medicine, Kansas City, Mo., USA,;(6) Vision Sciences Laboratory, University of Missouri School of Medicine, Kansas City, Mo., USA,;(7) Molecular Biology Laboratory, The Children's Mercy Hospital, University of Missouri School of Medicine, Kansas City, Mo., USA,;(8) The Eye Foundation of Kansas City, University of Missouri School of Medicine, Kansas City, Mo., USA,;(9) Kapiolani Medical Center for Women and Children, Honolulu, Hawaii, USA,;(10) The Children's Regional Hospital, Cooper Hospital/University of Medicine and Dentistry of New Jersey, Camden, N.J., USA,;(11) Departments of Genetics, Research Institute and Pediatric Laboratory Medicine, Hospital for Sick Children, and the Department of Molecular and Medical Genetics, University of Toronto, Ontario, Canada,
Abstract:
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