Novel deletion in the ACTA1 gene associated with milder phenotype of nemaline myopathy in Chinese patient: a case reportLi Yang,Xin Mu,Qiuyan Shen,Dan Zhang,Yanming XuNEUROLOGICAL SCIENCES(2021)引用 0|浏览10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