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Where are the missing gene defects in inherited retinal disorders? : intronic and synonymous variants contribute at least to 4% of CACNA1F-mediated inherited retinal disorders
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Mutations in C8orf37, encoding a ciliary protein, are associated with autosomal-recessive retinal dystrophies with early macular involvement
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Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness
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Implantation of ultrathin, biofunctionalized polyimide membranes into the subretinal space of rats
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IQCB1 Mutations in Patients with Leber Congenital Amaurosis
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Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response
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Genotyping microarray for CSNB-associated genes