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首页> 外文期刊>Neurology: Official Journal of the American Academy of Neurology >An interrupted 34-CAG repeat SCA-2 allele in patients with sporadic spinocerebellar ataxia.
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An interrupted 34-CAG repeat SCA-2 allele in patients with sporadic spinocerebellar ataxia.

机译:一个中断34-CAG重复SCA-2等位基因零星的脊髓小脑的共济失调患者。

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摘要

In spinocerebellar ataxia type 2 (SCA-2), a difference of three CAG repeats distinguishes normal alleles (14 to 31 repeats) from pathogenic alleles (34 to 57 repeats). All sequenced pathogenic alleles have a pure CAG repeat structure, whereas interrupted repeats have been seen exclusively in normal alleles. The authors present two patients with sporadic SCA with an interrupted 34-CAG repeat allele, (CAG)24(CAA)(CAG)9, who showed a phenotype compatible with SCA-2. The interrupted allele coding for a 34 pure polyglutamine tract may cause the SCA phenotype.
机译:在脊髓小脑的共济失调2型(SCA-2)差三个CAG重复区分正常等位基因从致病(14 - 31日重复)57重复等位基因(34)。致病性等位基因纯CAG重复结构,而打断了重复看到只在正常等位基因。现在两个零星的SCA患者打断34-CAG重复等位基因,(CAG) 24 (CAA) (CAG) 9日显示表型与SCA-2兼容。受到多麸醯胺酸编码34纯束导致SCA表型。

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