Clinical and Genetic (Whole Exome Sequences) Analysis of Retinopathy of Prematurity
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https://www.ncbi.nlm.nih.gov/sra/SRP277810
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资源简介：
Retinopathy of prematurity (ROP) 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. 100 samples have been selected for WES and all have been genotyped.
创建时间：
2024-02-21
