金子兵：Patient iPSC-derived retinal organoids for disease modeling
Currently, about 1/4 highly myopic patients can be identified monogenic mutations, which allowed us to know the genetic spectrum of this disease. Over a decade, we have successfully established a new strategy of trio-based exome seq and identified several new causal genes in childhood patients. Afterward, we performed a large-scale screening in adult patients. Then we found a group of nonhuman primates with super-high myopia, with which we are doing a new intervention based on the current understanding on this disease.
来源：首都医学科学创新中心
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