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25. Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2). Vithana EN; Morgan P; Sundaresan P; Ebenezer ND; Tan DT; Mohamed MD; Anand S; Khine KO; Venkataraman D; Yong VH; Salto-Tellez M; Venkatraman A; Guo K; Hemadevi B; Srinivasan M; Prajna V; Khine M; Casey JR; Inglehearn CF; Aung T Nat Genet; 2006 Jul; 38(7):755-7. PubMed ID: 16767101 [TBL] [Abstract][Full Text] [Related]
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31. Delayed onset of congenital hereditary endothelial dystrophy due to compound heterozygous SLC4A11 mutations. Kumawat BL; Gupta R; Sharma A; Sen S; Gupta S; Tandon R Indian J Ophthalmol; 2016 Jul; 64(7):492-5. PubMed ID: 27609159 [TBL] [Abstract][Full Text] [Related]
33. Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy. Desir J; Moya G; Reish O; Van Regemorter N; Deconinck H; David KL; Meire FM; Abramowicz MJ J Med Genet; 2007 May; 44(5):322-6. PubMed ID: 17220209 [TBL] [Abstract][Full Text] [Related]
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