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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Autori principali: Abouzeid, Hana, Youssef, Mohamed A., ElShakankiri, Nihal, Hauser, Philippe, Munier, Francis L., Schorderet, Daniel F.
Natura: Artigo
Lingua:Inglês
Pubblicazione: Molecular Vision 2009
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Research Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC2765237/
https://ncbi.nlm.nih.gov/pubmed/19862335
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