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Year | Number of Results |
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1998 | 2 |
2010 | 1 |
2015 | 1 |
2016 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 9187
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Next-generation sequencing confirms the implication of SLC24A1 in autosomal-recessive congenital stationary night blindness.
Clin Genet. 2016 Jun;89(6):690-9. doi: 10.1111/cge.12746. Epub 2016 Mar 4.
Clin Genet. 2016.
PMID: 26822852
A new mouse model for stationary night blindness with mutant Slc24a1 explains the pathophysiology of the associated human disease.
Vinberg F, Wang T, Molday RS, Chen J, Kefalov VJ.
Vinberg F, et al.
Hum Mol Genet. 2015 Oct 15;24(20):5915-29. doi: 10.1093/hmg/ddv319. Epub 2015 Aug 5.
Hum Mol Genet. 2015.
PMID: 26246500
Free PMC article.
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A mutation in SLC24A1 implicated in autosomal-recessive congenital stationary night blindness.
Riazuddin SA, Shahzadi A, Zeitz C, Ahmed ZM, Ayyagari R, Chavali VR, Ponferrada VG, Audo I, Michiels C, Lancelot ME, Nasir IA, Zafar AU, Khan SN, Husnain T, Jiao X, MacDonald IM, Riazuddin S, Sieving PA, Katsanis N, Hejtmancik JF.
Riazuddin SA, et al.
Am J Hum Genet. 2010 Oct 8;87(4):523-31. doi: 10.1016/j.ajhg.2010.08.013. Epub 2010 Sep 16.
Am J Hum Genet. 2010.
PMID: 20850105
Free PMC article.
Item in Clipboard
Chromosomal localization and genomic organization of the human retinal rod Na-Ca+K exchanger.
Tucker JE, Winkfein RJ, Murthy SK, Friedman JS, Walter MA, Demetrick DJ, Schnetkamp PP.
Tucker JE, et al.
Hum Genet. 1998 Oct;103(4):411-4. doi: 10.1007/s004390050842.
Hum Genet. 1998.
PMID: 9856482
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cDNA cloning of the human retinal rod Na-Ca + K exchanger: comparison with a revised bovine sequence.
Tucker JE, Winkfein RJ, Cooper CB, Schnetkamp PP.
Tucker JE, et al.
Invest Ophthalmol Vis Sci. 1998 Feb;39(2):435-40.
Invest Ophthalmol Vis Sci. 1998.
PMID: 9478004
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