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1)  spinocerebellar ataxia type 3
脊髓小脑型共济失调Ⅲ型
1.
Objective This study sought to isolate and identify the proteins that interact with ataxin-3, to confirm the interacted domain, and to provide new clues for exploring the function of ataxin-3 and the pathogenesis of spinocerebellar ataxia type 3 and Machado-Joseph disease (SCA3/MJD).
目的筛选ataxin3的相互作用蛋白并进行互作结构域分析,探讨ataxin3的功能和脊髓小脑型共济失调Ⅲ型/马查多约瑟夫病的发病机理。
2)  spinocerebellar ataxia type 1
脊髓小脑共济失调1型
1.
Clinical analysis on the cases with intermediate Cytosine-Adenine-Guanine repeat alleles of spinocerebellar ataxia type 1;
脊髓小脑共济失调1型中等重复动态突变患者临床表型分析
3)  spinocerebellar ataxia type2
脊髓小脑共济失调2型
1.
Clinical characteristics and MRI features of 8 spinocerebellar ataxia type2 and type3 patients;
8例脊髓小脑共济失调2型、3型患者的临床表型及MRI表现分析
4)  spinocerebellar ataxia
脊髓小脑型共济失调
1.
Clinical characteristics and genetic diagnosis of hereditary spinocerebellar ataxia type 7;
遗传性脊髓小脑型共济失调7型遗传学诊断及临床特征
5)  Spinocercbellar ataxia type 3
脊髓小脑共济失调3型
1.
Objective: To detect the clinical features of patients of Spinocercbellar ataxia type 3 (SCA3/MJD),we knowed its clinical characteristics detailedly.
目的:通过对新疆脊髓小脑共济失调3型(SCA3/MJD)家系患者的临床表现的调查,了解其临床特点,并对家系成员及患者进行基因分析,进而研究该疾病临床表现与基因突变的关系,同时作出基因诊断和症状前诊断。
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6)  spinocerebellar ataxia type 3 and Machado-Joseph disease(SCA3/MJD)
脊髓小脑型共济失调Ⅲ型/马查多-约瑟夫病
补充资料：脊髓遗传型共济失调


脊髓遗传型共济失调


　　即"脊髓型共济失调"。
　　
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
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