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ABCA4 variant screening in a Turkish cohort with Stargardt disease.

Neslihan Sinim KahramanBüşra Özgüç ÇalışkanNefise KandemirAyşe ÖnerMunis DündarYusuf Ozkul
Published in: Ophthalmic genetics (2024)
In this study, two novel variants were described in a Turkish cohort with Stargardt disease. The variant c.52C>T p.(Arg18Trp) was the most common disease-causing variant besides the c.5882 G>A p.(Gly1961Glu) which was identified frequently in the previous studies. A larger sample size is necessary for describing different pathogenic variants and understanding the phenotype-genotype correlations.
Keyphrases
  • copy number
  • gene expression
  • dna methylation