Harel Yoon syndrome: a novel mutation in ATAD3A gene and expansion of the clinical spectrum.
Caroline Atef TawfikRaghda ZaitounAliaa Ahmed FaragPublished in: Ophthalmic genetics (2023)
Our study reports a novel mutation in ATAD3A gene and expands the clinical spectrum of Harel-Yoon Syndrome. Future research aiming at better understanding of gene function will lead to better genotype-phenotype correlation and could pave the way to more treatment options.