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Goldmann-Favre Syndrome: Case Series
Goldmann-Favre syndrome, which is caused by mutation of the NR2E3 gene, is a retinal degenerative disease with a wide spectrum of phenotypic properties. Variations in clinical presentation result in difficulties in differential diagnosis. In this article, Goldmann-Favre syndrome cases with different...
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| Publicado no: | Turk J Ophthalmol |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Galenos Publishing
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5854860/ https://ncbi.nlm.nih.gov/pubmed/29576899 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4274/tjo.76158 |
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