Related Articles

• Detection of CRB1 mutations in families with retinal dystrophy through phenotype-oriented mutational screening
• Identification of CRB1 mutations in two Chinese consanguineous families exhibiting autosomal recessive retinitis pigmentosa
• Exome sequencing reveals CHM mutations in six families with atypical choroideremia initially diagnosed as retinitis pigmentosa
• Compound pathogenic mutation in the USH2A gene in Chinese RP families detected by whole‑exome sequencing
• RGR variants in different forms of retinal diseases: The undetermined role of truncation mutations