Clinical and genetic analysis of retinopathy of prematurity
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Retinopathy of prematurity is a leading cause of childhood blindness worldwide and is treated based on the presence of symptoms of “plus disease,” a dilation and tortuosity of retinal vessels. This project aims to identify the genetic and clinical underpinnings of the disease by comparing the germline variants of ~1,400 premature babies.
创建时间：
2020-04-04
