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...

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Detalles Bibliográficos
Autores principales: El Matri, Leila, Ouechtati, Farah, Chebil, Ahmed, Largueche, Leila, Abdelhak, Sonia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ophthalmic Research Center 2013
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3957041/
https://www.ncbi.nlm.nih.gov/pubmed/24653822

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3957041/
https://www.ncbi.nlm.nih.gov/pubmed/24653822

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