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PAX6 aniridia and interhemispheric brain anomalies

PURPOSE: To report the clinical and genetic study of patients with autosomal dominant aniridia. METHODS: We studied ten patients with aniridia from three families of Egyptian origin. All patients underwent full ophthalmologic, general and neurological examination, and blood drawing. Cerebral magneti...

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Detalles Bibliográficos
Autores principales:	Abouzeid, Hana, Youssef, Mohamed A., ElShakankiri, Nihal, Hauser, Philippe, Munier, Francis L., Schorderet, Daniel F.
Formato:	Texto
Lenguaje:	English
Publicado:	Molecular Vision 2009
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2765237/ https://www.ncbi.nlm.nih.gov/pubmed/19862335

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