BEST1-related autosomal dominant vitreoretinochoroidopathy: a degenerative disease with a range of developmental ocular anomalies.

Vincent, A; McAlister, C; Vandenhoven, C; Héon, E

Vincent, A; McAlister, C; Vandenhoven, C; Héon, E.

Affiliation

Vincent A; Department of Ophthalmology and Vision Sciences, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.

Eye (Lond) ; 25(1): 113-8, 2011 Jan.

Article in En | MEDLINE | ID: mdl-21072067

Subject(s)

Choroid Diseases/physiopathology; Eye/pathology; Retinal Diseases/physiopathology; Adult; Bestrophins; Chloride Channels/genetics; Choroid Diseases/genetics; Electrophysiology; Eye Proteins/genetics; Female; Follow-Up Studies; Humans; Male; Middle Aged; Mutation; Phenotype; Retinal Diseases/genetics; Retrospective Studies; Sequence Analysis, DNA; Visual Acuity/physiology; Visual Fields/physiology

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Retinal Diseases / Choroid Diseases / Eye Type of study: Observational_studies / Prognostic_studies Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Eye (Lond) Year: 2011 Document type: Article

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