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Corneal Dystrophy, Juvenile Epithelial of Meesmann

"Corneal Dystrophy, Juvenile Epithelial of Meesmann" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

An autosomal dominant form of hereditary corneal dystrophy due to a defect in cornea-specific KERATIN formation. Mutations in the genes that encode KERATIN-3 and KERATIN-12 have been linked to this disorder.


This graph shows the total number of publications written about "Corneal Dystrophy, Juvenile Epithelial of Meesmann" by people in Harvard Catalyst Profiles by year, and whether "Corneal Dystrophy, Juvenile Epithelial of Meesmann" was a major or minor topic of these publication.
Bar chart showing 1 publications over 1 distinct years, with a maximum of 1 publications in 2017
To see the data from this visualization as text, click here.
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.