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Clinical characterisation of the CABP4-related retinal phenotype
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Clinical characterisation of the CABP4-related retinal phenotype

Khan AO, Alrashed M, Alkuraya FS and may alrashed

Abstract

Calcium-Binding Proteins Chromosomes, Human, Pair 11 Codon, Nonsense Electroretinography Genotype Homozygote Night Blindness Pedigree Phenotype Photic Stimulation Photoreceptor Cells, Vertebrate Polymorphism, Single Nucleotide Retinal Degeneration RNA, Messenger Siblings Synapses Visual Field Tests

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