The c.794C > T p.(Ala265Val) SCN4A variant may be associated with congenital myopathy with FSHD-like phenotypeBarbora Plevova,Jana Zidkova,Petra Lassuthova,Roope Mannikko,Jana HaberlovaEUROPEAN JOURNAL OF HUMAN GENETICS(2022)引用 0|浏览12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