Spinocerebellar ataxia 13 is a slowly progressive and relatively pure autosomal dominant cerebellar ataxia with childhood onset and mental deficiency. The responsible gene has been assigned to a 5.2 Mbases interval on chromosome 19q in a single French family.
机构:
Univ Niigata, Dept Pathol, Brain Res Inst, Chuo Ku, 1-757 Asahimachi Dori, Niigata, JapanUniv Niigata, Dept Pathol, Brain Res Inst, Chuo Ku, 1-757 Asahimachi Dori, Niigata, Japan
Toyoshima, Yasuko
Takahashi, Hitoshi
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Univ Niigata, Dept Pathol, Brain Res Inst, Chuo Ku, 1-757 Asahimachi Dori, Niigata, JapanUniv Niigata, Dept Pathol, Brain Res Inst, Chuo Ku, 1-757 Asahimachi Dori, Niigata, Japan
机构:
Tokyo Med & Dent Univ, Ctr Personalized Med Hlth Aging, Bunkyo Ku, Tokyo, Japan
Tokyo Med & Dent Univ, Grad Sch Med & Dent Sci, Dept Neurol & Neurol Sci, Bunkyo Ku, Tokyo, JapanTokyo Med & Dent Univ, Ctr Personalized Med Hlth Aging, Bunkyo Ku, Tokyo, Japan
机构:
Federal University of Paraná,Movement Disorders Unit, Neurology Service, Hospital de ClínicasFederal University of Paraná,Movement Disorders Unit, Neurology Service, Hospital de Clínicas
Hélio A. Ghizoni Teive
Léo Coutinho
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Federal University of Paraná,Neurological Diseases Group, Postgraduate Program in Internal Medicine, Department of Internal Medicine, Hospital de ClínicasFederal University of Paraná,Movement Disorders Unit, Neurology Service, Hospital de Clínicas
Léo Coutinho
Carlos Henrique F. Camargo
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机构:Federal University of Paraná,Movement Disorders Unit, Neurology Service, Hospital de Clínicas