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Novel Norrie disease gene mutations in Chinese patients with familial exudative vitreoretinopathy
PURPOSE: This study aims to analyze the Norrie disease gene (NDP) variants in patients with familial exudative vitreoretinopathy (FEVR) and their clinical features. METHODS: Thirty-three Chinese patients (22 familial and 11 simplex) who were diagnosed as FEVR underwent detailed ocular examinations i...
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| Vydáno v: | BMC Ophthalmol |
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| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2021
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7885586/ https://ncbi.nlm.nih.gov/pubmed/33588793 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12886-021-01852-3 |
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