To identify the genetic defect in a Belgian family with congenital stromal corneal dystrophy.status: publishe
To identify the mutation of the TGFBI gene in Chinese patients with Reis-Bücklers corneal dystrophy,...
Purpose: To report a novel V505D mutation of the human transforming growth factor beta-induced (TGFB...
PURPOSE: Meesmann corneal dystrophy (MECD) is an autosomal dominant disorder affecting the corneal e...
Congenital hereditary stromal dystrophy (CHSD) of the cornea is a rare disease inherited in an autos...
PURPOSE. To describe the clinical and pathologic characteristics of a family with a congenital strom...
PURPOSE: To report a new family belonging to a previously non-investigated geographic are a with...
Purpose: Schnyder crystalline corneal dystrophy (SCCD) is an autosomal dominant disease characterize...
AIMS: To identify the underlying mutations in our British families and sporadic patients with dif...
PURPOSE: To identify the molecular defect causing gelatinous drop-like corneal dystrophy in a Turkis...
AIM: To report a phenotypic variant pedigree of lattice corneal dystrophy (LCD) associated with two ...
Background/Aims. Corneal dystrophies (CDs) belong to a group of hereditary heterogeneous corneal dis...
Corneal stromal dystrophies are a group of inherited disorders of the cornea that are caused by prog...
PURPOSE: Mutations in the BIGH3 gene on chromosome 5q31 cause four distinct autosomal dominant corne...
PURPOSE: To investigate the molecular basis of hereditary lattice corneal dystrophy (LCD) type IIIA ...
Towards the correction of genetic defect in corneal keratinocytes from patient with macular corneal ...
To identify the mutation of the TGFBI gene in Chinese patients with Reis-Bücklers corneal dystrophy,...
Purpose: To report a novel V505D mutation of the human transforming growth factor beta-induced (TGFB...
PURPOSE: Meesmann corneal dystrophy (MECD) is an autosomal dominant disorder affecting the corneal e...
Congenital hereditary stromal dystrophy (CHSD) of the cornea is a rare disease inherited in an autos...
PURPOSE. To describe the clinical and pathologic characteristics of a family with a congenital strom...
PURPOSE: To report a new family belonging to a previously non-investigated geographic are a with...
Purpose: Schnyder crystalline corneal dystrophy (SCCD) is an autosomal dominant disease characterize...
AIMS: To identify the underlying mutations in our British families and sporadic patients with dif...
PURPOSE: To identify the molecular defect causing gelatinous drop-like corneal dystrophy in a Turkis...
AIM: To report a phenotypic variant pedigree of lattice corneal dystrophy (LCD) associated with two ...
Background/Aims. Corneal dystrophies (CDs) belong to a group of hereditary heterogeneous corneal dis...
Corneal stromal dystrophies are a group of inherited disorders of the cornea that are caused by prog...
PURPOSE: Mutations in the BIGH3 gene on chromosome 5q31 cause four distinct autosomal dominant corne...
PURPOSE: To investigate the molecular basis of hereditary lattice corneal dystrophy (LCD) type IIIA ...
Towards the correction of genetic defect in corneal keratinocytes from patient with macular corneal ...
To identify the mutation of the TGFBI gene in Chinese patients with Reis-Bücklers corneal dystrophy,...
Purpose: To report a novel V505D mutation of the human transforming growth factor beta-induced (TGFB...
PURPOSE: Meesmann corneal dystrophy (MECD) is an autosomal dominant disorder affecting the corneal e...
DOI
Add to ORKG