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Burstedt, Marie S
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Bothnia dystrophy, a clinical, genetical and electrophysiological study
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Novel mutations in CRB1 and ABCA4 genes cause Leber congenital amaurosis and Sta...
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Mutation Spectra in Autosomal Dominant and Recessive Retinitis Pigmentosa in Nor...
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Mutation Spectra in Autosomal Dominant and Recessive Retinitis Pigmentosa in Nor...
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EYS mutations and implementation of minigene assay for variant classification in...
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EYS mutations and implementation of minigene assay for variant classification in...
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