Article

Energy Shortage in Human and Mouse Models of <i>SLC4A11</i> -Associated Corneal Endothelial Dystrophies

2019-12-08

Abstract excerpt

<h4> P urpose </h4> To elucidate the molecular events in solute carrier family 4 member 11 (SLC4A11)-deficient corneal endothelium that lead to the endothelial dysfunction that characterizes the dystrophies associated with SLC4A11 mutations, congenital hereditary endothelial dystrophy (CHED) and Fuchs endothelial corneal dystrophy 4. <h4> M ethods </h4> Comparative transcriptomic analysis (CTA) was perform...

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Literature Corpus work: a52da522-d0f5-58dc-91e6-fff55b8d9028
DOI: 10.1101/868281

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