ABCA4 variant screening in a Turkish cohort with Stargardt disease.
Neslihan Sinim KahramanBüşra Özgüç ÇalışkanNefise KandemirAyşe ÖnerMunis DündarYusuf OzkulPublished 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.