Ontology highlight
ABSTRACT:
SUBMITTER: Nikitina AS
PROVIDER: S-EPMC6558234 | biostudies-literature | 2019 Aug
REPOSITORIES: biostudies-literature
Nikitina Anastasia S AS Belodedova Alexandra V AV Malyugin Boris E BE Sharova Elena I EI Kostryukova Elena S ES Larin Andrey K AK Veselovsky Vladimir A VA Antonova Olga P OP Skorodumova Liubov O LO
Data in brief 20190523
Fuchs endothelial corneal dystrophy (FECD) is a bilateral inherited eye disease with advanced forms only treatable by corneal transplantation. The pathogenesis of FECD has not been worked out yet, however, trinucleotide repeat polymorphism CTG18.1 in the TCF4 gene has recently been associated with late-onset FECD. Gene expression profiling of corneal endothelium with and without this expansion can help elucidate molecular mechanisms of the disease development. Current data article represents who ...[more]