VSX1 and SOD1 Mutation Screening in Patients with Keratoconus in the South of Iran.

CONCLUSION: Mutations in VSX1 and SOD1 genes associated with keratoconus were not identified in our patients. Therefore, it will be necessary to investigate other chromosomal loci for potential causal mutations of keratoconus using next generation sequencing (NGS) methods in our population. PMID: 28540003 [PubMed - in process]
Source: Journal of Ophthalmic and Vision Research - Category: Opthalmology Tags: J Ophthalmic Vis Res Source Type: research