OMIM/217700[Secondary Source ID] - Search Results

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Genetic analysis of two Indian families affected with congenital hereditary endothelial dystrophy: two novel mutations in SLC4A11.

Kumar A, Bhattacharjee S, Prakash DR, Sadanand CS. Kumar A, et al. Mol Vis. 2007 Jan 16;13:39-46. Mol Vis. 2007. PMID: 17262014 Free PMC article.

Genomic organization of human CDS2 and evaluation as a candidate gene for corneal hereditary endothelial dystrophy 2 on chromosome 20p13.

Halford S, Inglis S, Gwilliam R, Spencer P, Mohamed M, Ebenezer ND, Hunt DM. Halford S, et al. Exp Eye Res. 2002 Nov;75(5):619-23. doi: 10.1006/exer.2002.2052. Exp Eye Res. 2002. PMID: 12457874 No abstract available.

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