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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...
Autores principales: | Rajendran, Rahini, Sudha, Dhandayuthapani, Chidambaram, Subbulakshmi, Nagarajan, Hemavathy, Vetrivel, Umashankar, Arunachalam, Jayamuruga Pandian |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
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 |
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