# Precision ophthalmology: a call for Africa not to be left in the dark

**Authors:** Lisa Roberts

PMC · DOI: 10.1038/s41434-024-00448-y · 2024-03-22

## Full-text entities

- **Genes:** BBS10 (Bardet-Biedl syndrome 10) [NCBI Gene 79738] {aka C12orf58}, MYO7A (myosin VIIA) [NCBI Gene 4647] {aka DFNA11, DFNB2, MYOVIIA, MYU7A, NSRD2, USH1B}, RPE65 (retinoid isomerohydrolase RPE65) [NCBI Gene 6121] {aka BCO3, LCA2, RP20, mRPE65, p63, rd12}, CEP290 (centrosomal protein 290) [NCBI Gene 80184] {aka 3H11Ag, BBS14, CT87, JBTS5, LCA10, MKS4}
- **Diseases:** Usher syndrome (MESH:D052245), eye diseases (MESH:D005128), blindness (MESH:D001766), IRD (MESH:D052919), IRDs (MESH:D057130), Mendelian disorders (MESH:D025861), vision loss (MESH:D014786), Bardet-Biedl syndrome (MESH:D020788), chorioretinal atrophy (MESH:C566236), Rare Disease (MESH:D035583)
- **Chemicals:** silver (MESH:D012834), EDIT-101 (-), gold (MESH:D006046), AON (MESH:D016376), oligonucleotide (MESH:D009841)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** c.2991+1655A>G

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Source: https://tomesphere.com/paper/PMC11090780