Whole-exome sequencing in a cohort of high myopia patients in northwest China

A total of 201 potential variants were identified in 27 families: 139 ones were well cosegregated with the disease in 15 families. Sixty-two variants were not cosegregated

本研究共在27个家系中鉴定出201个潜在变异，其中15个家系的139个变异与疾病呈现良好的共分离特征，剩余62个变异未表现出共分离现象。