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Absence of phenotype-genotype correlation of patients expressing mutations in the SLC4A11 gene.
Cornea. 2010 Mar;29(3):302-6. doi: 10.1097/ICO.0b013e3181ae9038.
Cornea. 2010.
PMID: 20118786
Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2).
Vithana EN, Morgan P, Sundaresan P, Ebenezer ND, Tan DT, Mohamed MD, Anand S, Khine KO, Venkataraman D, Yong VH, Salto-Tellez M, Venkatraman A, Guo K, Hemadevi B, Srinivasan M, Prajna V, Khine M, Casey JR, Inglehearn CF, Aung T.
Vithana EN, et al. Among authors: hemadevi b.
Nat Genet. 2006 Jul;38(7):755-7. doi: 10.1038/ng1824. Epub 2006 Jun 11.
Nat Genet. 2006.
PMID: 16767101
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Identification of mutations in the SLC4A11 gene in patients with recessive congenital hereditary endothelial dystrophy.
Hemadevi B, Veitia RA, Srinivasan M, Arunkumar J, Prajna NV, Lesaffre C, Sundaresan P.
Hemadevi B, et al.
Arch Ophthalmol. 2008 May;126(5):700-8. doi: 10.1001/archopht.126.5.700.
Arch Ophthalmol. 2008.
PMID: 18474783
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Genetic analysis of patients with Fuchs endothelial corneal dystrophy in India.
Hemadevi B, Srinivasan M, Arunkumar J, Prajna NV, Sundaresan P.
Hemadevi B, et al.
BMC Ophthalmol. 2010 Feb 10;10:3. doi: 10.1186/1471-2415-10-3.
BMC Ophthalmol. 2010.
PMID: 20144242
Free PMC article.
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