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Article

Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)

11 Jun 2006

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 16767101
DOI: 10.1038/ng1824

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Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)PMID 16767101Read ↗

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Multifunctional ion transport properties of human SLC4A11: comparison of the SLC4A11-B and SLC4A11-C variants.Semantic proximity Read ↗

Mutational spectrum of SLC4A11 in autosomal recessive CHED in Saudi Arabia.Semantic proximity Read ↗

SLC4A11 Revisited: Isoforms, Expression, Functions and Unresolved QuestionsSemantic proximity Read ↗

Identifications and in silico analysis of a spectrum of SLC4A11 mutations in Indian familial and non-familial cases of congenital hereditary endothelial dystrophySemantic proximity Read ↗

Sodium bicarbonate cotransporter NBCe2 gene variants increase sodium and bicarbonate transport in human renal proximal tubule cells.Semantic proximity Read ↗

Novel SLC4A11 mutations in patients with recessive congenital hereditary endothelial dystrophy (CHED2). Mutation in brief #958. Online.Semantic proximity Read ↗

Congenital hereditary endothelial dystrophy - mutation analysis of SLC4A11 and genotype-phenotype correlation in a North Indian patient cohort.Semantic proximity Read ↗

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