Associated Papers
Autosomal dominant stromal corneal dystrophy associated with a SPARCL1 missense variant.
Braddock FL et al.
European Journal of Human Genetics : Ejhg, 2024
Congenital stromal corneal dystrophy in a Spanish family: Clinical, genetic and histological analysis.
Gómez-Calleja V et al.
Journal Francais D'ophtalmologie, 2024
Novel DCN Mutation in Armenian Family With Congenital Stromal Corneal Dystrophy.
Williams D et al.
Cornea, 2023
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