脊髓小脑共济失调
神经退行性变
共济失调
遗传学
生物
神经科学
三核苷酸重复扩增
疾病
医学
基因
等位基因
病理
标识
DOI:10.1097/01.wco.0000084230.82329.d5
摘要
Mapping of additional ataxia loci and identification of novel ataxia genes continues unabated. Genetic classification enables typology of inherited ataxias. Identification of the affected loci and the mutational mechanisms has allowed the first glimmers of understanding of the pathogenesis of several inherited ataxias.
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