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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Detalles Bibliográficos
Autores principales: Rajendran, Rahini, Sudha, Dhandayuthapani, Chidambaram, Subbulakshmi, Nagarajan, Hemavathy, Vetrivel, Umashankar, Arunachalam, Jayamuruga Pandian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research Note
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8157631/
https://www.ncbi.nlm.nih.gov/pubmed/34039417
http://dx.doi.org/10.1186/s13104-021-05617-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8157631/
https://www.ncbi.nlm.nih.gov/pubmed/34039417
http://dx.doi.org/10.1186/s13104-021-05617-5

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