A relatively common cause of hereditary motor neuropathy due to a founder mutation in VWA1 S. Nagy, A. Pagnamenta,R. Maroofian,H. HouldenEUROPEAN JOURNAL OF NEUROLOGY(2023)引用 0|浏览8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