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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2007 | 2 |
2009 | 1 |
2014 | 1 |
2015 | 1 |
2024 | 0 |
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Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy.
J Med Genet. 2007 May;44(5):322-6. doi: 10.1136/jmg.2006.046904. Epub 2007 Jan 12.
J Med Genet. 2007.
PMID: 17220209
Free PMC article.
Mutational spectrum of the SLC4A11 gene in autosomal recessive congenital hereditary endothelial dystrophy.
Sultana A, Garg P, Ramamurthy B, Vemuganti GK, Kannabiran C.
Sultana A, et al.
Mol Vis. 2007 Jul 26;13:1327-32.
Mol Vis. 2007.
PMID: 17679935
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Mutational spectrum of SLC4A11 in autosomal recessive CHED in Saudi Arabia.
Aldahmesh MA, Khan AO, Meyer BF, Alkuraya FS.
Aldahmesh MA, et al.
Invest Ophthalmol Vis Sci. 2009 Sep;50(9):4142-5. doi: 10.1167/iovs.08-3006. Epub 2009 Apr 15.
Invest Ophthalmol Vis Sci. 2009.
PMID: 19369245
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Detailed assessment of renal function in a proband with Harboyan syndrome caused by a novel homozygous SLC4A11 nonsense mutation.
Liskova P, Dudakova L, Tesar V, Bednarova V, Kidorova J, Jirsova K, Davidson AE, Hardcastle AJ.
Liskova P, et al.
Ophthalmic Res. 2015;53(1):30-5. doi: 10.1159/000365109. Epub 2014 Dec 11.
Ophthalmic Res. 2015.
PMID: 25500497
Free article.
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