Associated Papers
A comprehensive molecular genetic analysis of keratoconus patients from assam, a northeastern state of India.
Chakravarty M et al.
European Journal of Ophthalmology, 2022
Investigating the Pathogenicity of VSX1 Missense Mutations and Their Association With Corneal Disease.
Litke AM et al.
Investigative Ophthalmology & Visual Science, 2018
Analysis of the VSX1 gene in sporadic keratoconus patients from China.
Guan T et al.
Bmc Ophthalmology, 2017
Two novel missense substitutions in the VSX1 gene: clinical and genetic analysis of families with Keratoconus from India.
Shetty R et al.
Bmc Medical Genetics, 2015
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