A de novo nonsense mutation in the N-terminal of ligand-binding domain of NR2F1 gene provoked a milder phenotype of BBSOASWenjun Zou,Libo Cheng,Shui Lu,Zhifeng WuOPHTHALMIC GENETICS(2020)引用 6|浏览3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