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2. Missense mutation in SLC4A11 in two Pakistani families affected with congenital hereditary endothelial dystrophy (CHED2). Kaul H; Suman M; Khan Z; Ullah MI; Ashfaq UA; Idrees S Clin Exp Optom; 2016 Jan; 99(1):73-7. PubMed ID: 26286922 [TBL] [Abstract][Full Text] [Related]
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