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Scholar Results 1 - 1 of 1 citing Hilton: De novo mutation in the BIGH3/TGFB1 gene causing granular corneal dystrophy. (0.06 sec) 

A novel phenotype-genotype relationship with a TGFBI exon 14 mutation in a pedigree with a …


CE Wheeldon, BH de Karolyi, DV Patel, T … - Molecular Vision, 2008 - pubmedcentral.nih.gov
Corneal dystrophy of Bowman's layer (CDB) belongs to a group of dystrophies
associated with mutations in the transforming growth factor-beta-induced (TGFBI)
gene. CDB is further divided into a geographic variant (CDB1/Reis ...
Cited by 1 - Related articles - All 6 versions


 


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