Associated Papers
Variants in CFAP410 cause a range of retinal and skeletal phenotypes.
Schmidt RE et al.
Npj Genomic Medicine, 2025
40246852 (PubMed )
Supplement: 41525_2025_489_MOESM1_ESM.pdf
Genetic Analysis of 252 Index Cases with Inherited Retinal Diseases Using a Panel of 351 Retinal Genes.
Abu Elasal M et al.
Genes, 2024
39062705 (PubMed )
Supplement: genes-15-00926-s001.zip › Table_S3.pdf
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