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Retinoschisis and Norrie disease: a missing link
OBJECTIVE: Retinoschisis and Norrie disease are X-linked recessive retinal disorders caused by mutations in RS1 and NDP genes respectively. Both are likely to be monogenic and no locus heterogeneity has been reported. However, there are reports showing overlapping features of Norrie disease and reti...
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| Publié dans: | BMC Res Notes |
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| Auteurs principaux: | , , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
BioMed Central
2021
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8157631/ https://ncbi.nlm.nih.gov/pubmed/34039417 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13104-021-05617-5 |
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