A new hereditary ataxia disorder with prominent cognitive impairment and 1C2 positive inclusionsL. Donker Kaat,J. G. J. van Rooij, S. Melhem,A. Verkerk,A. Rozemuller,J. C. van SwietenEUROPEAN JOURNAL OF HUMAN GENETICS(2018)引用 0|浏览14暂无评分AI 理解论文溯源树样例生成溯源树,研究论文发展脉络Chat Paper正在生成论文摘要