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24. Congenital hereditary endothelial dystrophy caused by SLC4A11 mutations progresses to Harboyan syndrome. Siddiqui S; Zenteno JC; Rice A; Chacón-Camacho O; Naylor SG; Rivera-de la Parra D; Spokes DM; James N; Toomes C; Inglehearn CF; Ali M Cornea; 2014 Mar; 33(3):247-51. PubMed ID: 24351571 [TBL] [Abstract][Full Text] [Related]
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