Novel homozygous nonsense PXDN mutation detected by whole exome sequencing causing anterior segment dysgenesis E. Kritioti,N. Nicolaou,A. Alexandrou, A. Syrimis, I. Papaevripidou,A. Theodosiou,V. Christophidou-Anastasiadou,C. Sismani,G. A. TantelesEUROPEAN JOURNAL OF HUMAN GENETICS(2019)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