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Clinical Polymorphism of Stargardt Disease in a Large Consanguineous Tunisian Family; Implications for Nosology
PURPOSE: To describe the polymorphic expression of Stargardt disease in a large Tunisian family with clinical intra- and interfamilial variation of the condition. METHODS: Twelve subjects from two related families with autosomal recessive Stargardt disease were enrolled. A detailed clinical examinat...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Ophthalmic Research Center
2013
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3957041/ https://www.ncbi.nlm.nih.gov/pubmed/24653822 |