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An Arg124Cys mutation in transforming growth factor β-induced gene associated with lattice corneal dystrophy type I in a Chinese pedigree
PURPOSE: To identify a clinical and genetic form of a large Chinese family with an autosomal-dominant lattice corneal dystrophy type I (LCD I). METHODS: The patients’ eyes were examined on the basis of slit-lamp microscopy, and other clinical records were also collected. Genomic DNA was extracted fr...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Wolters Kluwer - Medknow
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8917566/ https://www.ncbi.nlm.nih.gov/pubmed/34937214 http://dx.doi.org/10.4103/ijo.IJO_33_21 |