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TorsinA单倍体易患特发性肌张力障碍
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作者 Clarimon J. asgeirsson h. +2 位作者 Singleton A. S. Sveinbjornsdottir 袁海峰 《世界核心医学期刊文摘(神经病学分册)》 2005年第9期12-12,共1页
Previous work has suggested that in many neurological diseases genetic variabi lity in the loci predisposing subjects to autosomal dominant disease contributes to the risk of sporadic disease. Here, using a population... Previous work has suggested that in many neurological diseases genetic variabi lity in the loci predisposing subjects to autosomal dominant disease contributes to the risk of sporadic disease. Here, using a population-based sample of dyst onia cases, we show an association with the torsin A haplotype and sporadic idio pathic dystonia. 展开更多
关键词 TORSINA 肌张力障碍 神经系统疾病 发病风险 遗传变异
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