
Fuchs' endothelial corneal dystrophy (FECD) has been considered a genetically heterogeneous disease but is increasingly associated with the transcription factor 4 (TCF4) gene. This study investigates the prevalence of the cytosine‐thymine‐guanine (CTG)n repeat expansion in TCF4 among FECD patients in northern Sweden coupled to the phenotype. Blood samples were collected from 85 FECD cases at different stages. Short tandem repeat PCR and triplet repeat‐primed PCR were applied in order to determine TCF4 (CTG)n genotype...
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