Published in PLoS One on November 16, 2012
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A novel CACNA1F mutation in a french family with the incomplete type of X-linked congenital stationary night blindness. Am J Ophthalmol (2003) 0.93
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Combining gene mapping and phenotype assessment for fast mutation finding in non-consanguineous autosomal recessive retinitis pigmentosa families. Eur J Hum Genet (2011) 0.87
Identification of preferentially expressed mRNAs in retina and cochlea. DNA Cell Biol (2002) 0.87
Identification and quantification of phosphatidylcholines containing very-long-chain polyunsaturated fatty acid in bovine and human retina using liquid chromatography/tandem mass spectrometry. J Chromatogr A (2010) 0.87
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Dissecting the pathogenic mechanisms of mutations in the pore region of the human cone photoreceptor cyclic nucleotide-gated channel. Hum Mutat (2010) 0.81
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Screening for a canine model of choroideremia exclusively identifies nonpathogenic CHM variants. Ophthalmic Res (2010) 0.78
Early-onset foveal involvement in retinitis punctata albescens with mutations in RLBP1. JAMA Ophthalmol (2013) 0.78
Retinas of the diurnal rodent Arvicanthis ansorgei are highly resistant to experimentally induced stress and degeneration. Invest Ophthalmol Vis Sci (2011) 0.78
How can we prevent myopia progression? Eur J Ophthalmol (2015) 0.78