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27. Identification and in silico analysis of a spectrum of SLC4A11 variations in Indian familial and sporadic cases of congenital hereditary endothelial dystrophy. Salman M; Verma A; Chaurasia S; Prasad D; Kannabiran C; Singh V; Ramappa M Orphanet J Rare Dis; 2022 Sep; 17(1):361. PubMed ID: 36115991 [TBL] [Abstract][Full Text] [Related]
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