SLC4A11 and the Pathophysiology of Congenital Hereditary Endothelial Dystrophy

Congenital hereditary endothelial dystrophy (CHED) is a rare autosomal recessive disorder of the corneal endothelium characterized by nonprogressive bilateral corneal edema and opacification present at birth. Here we review the current knowledge on the role of the SLC4A11 gene, protein, and its muta...

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Bibliographic Details
Published in:Biomed Res Int
Main Authors: Patel, Sangita P., Parker, Mark D.
Format: Artigo
Language:Inglês
Published: Hindawi Publishing Corporation 2015
Subjects:
Review Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC4588344/
https://ncbi.nlm.nih.gov/pubmed/26451371
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2015/475392
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