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9. Mutation in the SLC4A11 gene associated with autosomal recessive congenital hereditary endothelial dystrophy in a large Saudi family. Shah SS; Al-Rajhi A; Brandt JD; Mannis MJ; Roos B; Sheffield VC; Syed NA; Stone EM; Fingert JH Ophthalmic Genet; 2008 Mar; 29(1):41-5. PubMed ID: 18363173 [TBL] [Abstract][Full Text] [Related]
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18. Fuchs Endothelial Corneal Dystrophy in a Heterozygous Carrier of Congenital Hereditary Endothelial Dystrophy Type 2 with a Novel Mutation in SLC4A11. Kim JH; Ko JM; Tchah H Ophthalmic Genet; 2015; 36(3):284-6. PubMed ID: 24502824 [TBL] [Abstract][Full Text] [Related]
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