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Clinical and Genetic Characterization of Autosomal Recessive Spinocerebellar Ataxia Type 16 (SCAR16) in Taiwan
Authors:Chiu  Hsu-Huai  Hsaio   Cheng-Tsung  Tsai   Yu-Shuen  Liao   Yi-Chu  Lee   Yi-Chung  Soong   Bing-Wen
Affiliation:1.Department of Neurology, Taipei Veterans General Hospital, Taipei, Taiwan
;2.Department of Neurology, National Yang-Ming University School of Medicine, Taipei, Taiwan
;3.Division of Neurology, Department of Internal Medicine, Taipei Veterans General Hospital Taoyuan Branch, Taoyuan, Taiwan
;4.Graduate Institute of Physiology, College of Medicine, National Taiwan University, Taipei, Taiwan
;5.Institute of Biomedical Informatics, National Yang-Ming University, Taipei, Taiwan
;6.Center for Systems and Synthetic Biology, National Yang-Ming University, Taipei, Taiwan
;7.Brain Research Center, National Yang-Ming University School of Medicine, Taipei, Taiwan
;8.Taipei Neuroscience Institute, Taipei Medical University, Taipei, Taiwan
;9.Department of Neurology, Taipei Medical University-Shuang Ho Hospital, New Taipei City, Taiwan
;
Abstract:The Cerebellum - Mutations in STUB1 have been identified to cause autosomal recessive spinocerebellar ataxia type 16 (SCAR16), also named as Gordon Holmes syndrome, which is characterized by...
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