Oculomotor and visual axis systems sparing in spinocerebellar ataxia type 13(R420H).
作者信息
Waters Michael F, Subramony Sankarasubramoney H, Advincula Joel, Perlman Susan, Ashizawa Tetsuo
机构信息
Department of Neurology, University of Florida College of Medicine, Gainesville, USA.
出版信息
Neurology. 2012 Sep 11;79(11):1181-2. doi: 10.1212/WNL.0b013e3182698d5c. Epub 2012 Aug 29.
Abstract
摘要
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Oculomotor and visual axis systems sparing in spinocerebellar ataxia type 13(R420H).13型脊髓小脑共济失调（R420H）中动眼神经和视轴系统未受累
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本文引用的文献
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An approach to the patient with late-onset cerebellar ataxia.迟发性小脑共济失调患者的诊疗方法。
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Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypes.电压门控钾通道KCNC3的突变会导致退行性和发育性中枢神经系统表型。
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Oculomotor phenotypes in autosomal dominant ataxias.常染色体显性共济失调中的动眼神经表型
Arch Neurol. 1998 Oct;55(10):1353-7. doi: 10.1001/archneur.55.10.1353.
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Classification of the hereditary ataxias and paraplegias.遗传性共济失调和截瘫的分类。
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