Ulrich Kellner
0000-0001-5221-4631
4 papers found
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Investigation of Structural Alterations in Inherited Retinal Diseases: A Quantitative SD-OCT-Analysis of Retinal Layer Thicknesses in Light of Underlying Genetic Mutations
The landscape of submicroscopic structural variants at the OPN1LW/OPN1MW gene cluster on Xq28 underlying blue cone monochromacy
Dominant mutations in mtDNA maintenance gene SSBP1 cause optic atrophy and foveopathy
Mutation spectrum and clinical investigation of achromatopsia patients with mutations in the GNAT2 gene
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