Associated Papers
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
A pediatric case of congenital stromal corneal dystrophy caused by the novel variant c.953del of the DCN gene.
Morikawa H et al.
Human Genome Variation, 2023
36964172 (PubMed )
Supplement: 41439_2023_239_MOESM2_ESM.xlsx › Sheet1
Variant Landscape of 15 Genes Involved in Corneal Dystrophies: Report of 30 Families and Comprehensive Analysis of the Literature.
Zhu D et al.
International Journal of Molecular Sciences, 2023
36902444 (PubMed )
Supplement: ijms-24-05012-s001.zip › ijms-2152855-Supplementary_Table_S4_.xlsx › Sheet1
Role of Decorin Core Protein in Collagen Organisation in Congenital Stromal Corneal Dystrophy (CSCD).
Kamma-Lorger CS et al.
Plos One, 2016
Regulation of corneal stroma extracellular matrix assembly.
Chen S et al.
Experimental Eye Research, 2015
Novel decorin mutation in a Chinese family with congenital stromal corneal dystrophy.
Jing Y et al.
Cornea, 2014
A novel decorin gene mutation in congenital hereditary stromal dystrophy: a Korean family.
Lee JH et al.
Korean Journal of Ophthalmology : Kjo, 2012
A novel mutation of the decorin gene identified in a Korean family with congenital hereditary stromal dystrophy.
Kim JH et al.
Cornea, 2011
A second decorin frame shift mutation in a family with congenital stromal corneal dystrophy.
Rødahl E et al.
American Journal of Ophthalmology, 2006
Congenital corneal opacities: a review with a focus on genetics.
Ciralsky J et al.
Seminars in Ophthalmology, 0
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