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Retinal Features of Family Members With Familial Exudative Vitreoretinopathy Caused By Mutations in KIF11 Gene
PURPOSE: To determine the clinical characteristics of patients and family members with familial exudative vitreoretinopathy (FEVR) caused by mutations in the KIF11 gene. METHODS: Twenty-one patients from 10 FEVR families with mutations in the KIF11 gene were studied. The retinal and systemic feature...
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| Publicat a: | Transl Vis Sci Technol |
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| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
The Association for Research in Vision and Ophthalmology
2021
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8212440/ https://ncbi.nlm.nih.gov/pubmed/34128965 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/tvst.10.7.18 |
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