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Case report: A case of Norrie disease due to deletion of the entire coding region of NDP gene
PURPOSE: Norrie disease is a rare X-linked recessive vitreoretinopathy. Variants of the NDP gene are associated with this condition. This case reports aims to demonstrate the variations of clinical presentations and exam findings of this disease. OBSERVATIONS: A retrospective chart review of the pat...
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| Udgivet i: | Am J Ophthalmol Case Rep |
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| Main Authors: | , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Elsevier
2021
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8220341/ https://ncbi.nlm.nih.gov/pubmed/34189345 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajoc.2021.101151 |
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