RNA Missplicing in Fuchs Endothelial Corneal Dystrophy
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ABSTRACT: RNA-Seq splicing data from the corneal endothelia of FECD patients and controls reveal hundreds of differential alternative splicing events. These include events previously characterized in the context of myotonic dystrophy type 1 and epithelial-to-mesenchymal transition, as well as splicing changes in genes related to proposed mechanisms of FECD pathogenesis
ORGANISM(S): Homo sapiens
PROVIDER: GSE101872 | GEO | 2017/07/26
SECONDARY ACCESSION(S): PRJNA395734
REPOSITORIES: GEO
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