| Autor: |
Ensieh, Darbari, Hamid, Ahmadieh, Narsis, Daftarian, Mozhgan, Rezaei Kanavi, Fatemeh, Suri, Hamideh, Sabbaghi, Elahe, Elahi |
| Rok vydání: |
2020 |
| Zdroj: |
Journal of ophthalmicvision research. 17(1) |
| ISSN: |
2008-2010 |
| Popis: |
Stargardt disease type 1 (STGD1) is a recessively inherited retinal disorder that can cause severe visual impairment.Eighteen STGD1 patients were recruited for genetic analysis. Diagnosis by retina specialists was based on standard criteria, including accumulation of lipofuscin. The sixOne or moreAs |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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