A family with Wagner syndrome with uveitis and a new versican mutation

PURPOSE: To report the clinical and molecular findings of a kindred with Wagner syndrome (WS) revealed by intraocular inflammatory features. METHODS: Eight available family members underwent complete ophthalmologic examination, including laser flare cell meter measurements. Collagen, type II, alpha...

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Detalles Bibliográficos
Autores principales: Rothschild, Pierre-Raphaël, Brézin, Antoine P., Nedelec, Brigitte, des Roziers, Cyril Burin, Ghiotti, Tiffany, Orhant, Lucie, Boimard, Mathieu, Valleix, Sophie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3811992/
https://www.ncbi.nlm.nih.gov/pubmed/24174867

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