Identification of a Novel Missense KRT12 Mutation in a Vietnamese Family with Meesmann Corneal Dystrophy
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DOI: 10.1159/000506435
Abstract: Meesmann epithelial corneal dystrophy (MECD) is a rare dominantly inherited disorder that is characterized by corneal epithelial microcysts and is associated with mutations in the keratin 3 (KRT3) and keratin 12 (KRT12) genes. In this… read more here.
Keywords: vietnamese family; corneal dystrophy; family; krt12 ... See more keywords