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Harel Yoon syndrome: a novel mutation in ATAD3A gene and expansion of the clinical spectrum.

Caroline Atef TawfikRaghda ZaitounAliaa Ahmed Farag
Published 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.
Keyphrases
  • copy number
  • genome wide
  • case report
  • emergency department
  • gene expression
  • dna methylation
  • current status