Analysis of gene mutation spectrum for early-onset high myopia based on whole-exome sequencing.

چکیده

This study aimed to identify the loci of gene mutations associated with high myopia, analyse the genetic mutation spectrum characteristics for early onset high myopia (eo-HM) and explore the application of polygenic risk scores (PRSs) in predicting eo-HM. Whole-exome sequencing (WES) and ophthalmic…

متن کامل چکیده در سایت ناشر در دسترس است.

موضوعات مرتبط

• نزدیک بینی