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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...

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Detalles Bibliográficos
Autores principales:	Li, Feng, He, Jiahuan, Bai, Hua, Huang, Yifei, Wang, Fang, Tian, Lei
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer - Medknow 2022
Materias:	Original Article
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

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