Genetic and clinical landscape of ARR3-associated MYP26: the most common cause of Mendelian early-onset high myopia with a unique inheritance

Abstract

AimsTo elucidate genetic background of early-onset high myopia (eoHM) and characteristics of ARR3-associated MYP26.MethodsVariants in 14 genes reported to contribute to eoHM, including ARR3, were selected from exome sequencing data...