2020.08.09
ハンチントン病におけるアレル選択的治療のための一塩基多型の遺伝子型決定
Genotyping single nucleotide polymorphisms for allele-selective therapy in Huntington disease
Daniel O Claassen1, Jody Corey-Bloom, E Ray Dorsey, Mary Edmondson, Sandra K Kostyk, Mark S LeDoux, Ralf Reilmann, H Diana Rosas, Francis Walker, Vicki Wheelock, Nenad Svrzikapa, Kenneth A Longo, Jaya Goyal, Serena Hung, Michael A Panzara
1From Vanderbilt University Medical Center (D.O.C.), Nashville, TN; University of California San Diego (J.C.-B.), La Jolla; University of Rochester Medical Center (E.R.D.), NY; HD Reach (M.E.), Raleigh, NC; Ohio State University (S.K.K.), Columbus; University of Memphis and Veracity Neuroscience, LLC (M.S.L.), TN; George-Huntingon-Institute & Department of Clinical Radiology University of Muenster (R.R.), Department of Neurodegeneration, Hertie Institute for Clinical Brain Research, University of Tuebingen, Germany; Havard Medical School (H.D.R.), Massachusetts General Hospital, Boston; Wake Forest University School of Medicine (F.W.), Winston Salem, NC; University of California Davis Health (V.W.), Sacramento, CA; Wave Life Sciences USA, Inc. (N.S., K.A.L., J.G., S.H., M.A.P.), Cambridge, MA; and Department of Paediatrics (N.S.), Medical Sciences Division, University of Oxford, UK.