reference/9266826

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startingPage	41
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bibliographicCitation	Shah SS, Al-Rajhi A, Brandt JD, Mannis MJ, Roos B, Sheffield VC, Syed NA, Stone EM, Fingert JH. Mutation in the SLC4A11 gene associated with autosomal recessive congenital hereditary endothelial dystrophy in a large Saudi family. Ophthalmic Genet. 2008 Mar;29(1):41–5. doi: 10.1080/13816810701850033. PMID: 18363173.
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date	200801
identifier	https://pubmed.ncbi.nlm.nih.gov/18363173 https://doi.org/10.1080/13816810701850033
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Mutation in theSLC4A11Gene Associated with Autosomal Recessive Congenital Hereditary Endothelial Dystrophy in a Large Saudi Family
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