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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Dades bibliogràfiques
Publicat a:BMC Res Notes
Autors principals: Rajendran, Rahini, Sudha, Dhandayuthapani, Chidambaram, Subbulakshmi, Nagarajan, Hemavathy, Vetrivel, Umashankar, Arunachalam, Jayamuruga Pandian
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2021
Matèries:
Research Note
Accés en línia: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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