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National Institutes of Health
Lattice corneal dystrophy Type I
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TGFBI (BIGH3) gene mutations in German families: two novel mutations associated with unique clinical and histopathological findings
British Journal of Ophthalmology
Corpus ID: 5358191
Background: To report the clinical, histopathological and immunohistochemical findings of two novel mutations within the TGFBI…
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