gene causing a lattice corneal dystrophy with deep stromal involvement Lattice corneal dystrophy (LCD) type I is one of the five dominant TGFBI (trans-formimg growth factor b induced; formerly designated as bigh3 or keratoepithelin)-related corneal dystrophies with character-istic lattice-like refractile lines in the corneal stroma.1 Other than this common-type LCD, there have also been reported several minor-type LCDs caused by different mutations of the TGFBI gene.2 CASE REPORT An 85-year-old man presented wit
Phenotypic characteristics associated with mutations in the tran- sforming growth factor beta-induce...
PURPOSE: To investigate the molecular basis of hereditary lattice corneal dystrophy (LCD) type IIIA ...
Phenotypic characteristics associated with mutations in the tran- sforming growth factor beta-induce...
A novel mutation of the TGFBI gene causing a lattice corneal dystrophy with deep stromal involvement...
Recent advances have allowed us to understand corneal dystrophies on a basic molecular level, and se...
AIM: To report a phenotypic variant pedigree of lattice corneal dystrophy (LCD) associated with two ...
Purpose To report the association of phenotypic features characteristic of lattice corneal dystroph...
Purpose: To report the clinical, ophthalmic, and genetic characteristics for lattice corneal dystrop...
Purpose: To report the clinical, ophthalmic, and genetic characteristics for lattice corneal dystrop...
Purpose: To report a novel V505D mutation of the human transforming growth factor beta-induced (TGFB...
PURPOSE: To characterize the molecular defect in the TGFBI gene in a Chinese family affected with an...
AIM: To explore the mutation type of TGFBI gene in a lattice-like corneal dystrophy(LCD)family in no...
PURPOSE: The aim of this study was to report a lattice corneal dystrophy (LCD) family with a novel m...
Phenotypic characteristics associated with mutations in the tran- sforming growth factor beta-induce...
PURPOSE: To investigate the molecular basis of hereditary lattice corneal dystrophy (LCD) type IIIA ...
Phenotypic characteristics associated with mutations in the tran- sforming growth factor beta-induce...
PURPOSE: To investigate the molecular basis of hereditary lattice corneal dystrophy (LCD) type IIIA ...
Phenotypic characteristics associated with mutations in the tran- sforming growth factor beta-induce...
A novel mutation of the TGFBI gene causing a lattice corneal dystrophy with deep stromal involvement...
Recent advances have allowed us to understand corneal dystrophies on a basic molecular level, and se...
AIM: To report a phenotypic variant pedigree of lattice corneal dystrophy (LCD) associated with two ...
Purpose To report the association of phenotypic features characteristic of lattice corneal dystroph...
Purpose: To report the clinical, ophthalmic, and genetic characteristics for lattice corneal dystrop...
Purpose: To report the clinical, ophthalmic, and genetic characteristics for lattice corneal dystrop...
Purpose: To report a novel V505D mutation of the human transforming growth factor beta-induced (TGFB...
PURPOSE: To characterize the molecular defect in the TGFBI gene in a Chinese family affected with an...
AIM: To explore the mutation type of TGFBI gene in a lattice-like corneal dystrophy(LCD)family in no...
PURPOSE: The aim of this study was to report a lattice corneal dystrophy (LCD) family with a novel m...
Phenotypic characteristics associated with mutations in the tran- sforming growth factor beta-induce...
PURPOSE: To investigate the molecular basis of hereditary lattice corneal dystrophy (LCD) type IIIA ...
Phenotypic characteristics associated with mutations in the tran- sforming growth factor beta-induce...
PURPOSE: To investigate the molecular basis of hereditary lattice corneal dystrophy (LCD) type IIIA ...
Phenotypic characteristics associated with mutations in the tran- sforming growth factor beta-induce...